Term with siblings
epidermolysis bullosa simplex with muscular dystrophy

2-aminoadipic 2-oxoadipic aciduria
3-M syndrome
3-M syndrome
3-Methylcrotonyl-CoA carboxylase deficiency +
3-methylglutaconic aciduria type 1
3-methylglutaconic aciduria type 3
3-methylglutaconic aciduria type 5
3-methylglutaconic aciduria type 8
3-methylglutaconic aciduria type 9
3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome
3MC syndrome +
3MC syndrome +
Aagenaes syndrome
ABCD syndrome
ABCD syndrome
abdominal obesity-metabolic syndrome +
abetalipoproteinemia
ablepharon macrostomia syndrome
aceruloplasminemia
achalasia microcephaly syndrome
achalasia microcephaly syndrome
Achard syndrome
acheiropody
achondrogenesis type IA
achondrogenesis type IB
achromatopsia 2
achromatopsia 3
achromatopsia 7
acrocallosal syndrome
acrocapitofemoral dysplasia
acromesomelic dysplasia, Grebe type
acromesomelic dysplasia, Hunter-Thompson type
acromesomelic dysplasia, Maroteaux type
acrorenal syndrome
Adams-Oliver syndrome
Adie syndrome
adult spinal muscular atrophy
ADULT syndrome
agammaglobulinemia 4
AGAT deficiency
agenesis of the corpus callosum with peripheral neuropathy
Aicardi syndrome
Aicardi-Goutieres syndrome
Alkuraya-Kucinskas syndrome
Alkuraya-Kucinskas syndrome
Allan-Herndon-Dudley syndrome
alopecia universalis
alpha-2-plasmin inhibitor deficiency
Alport syndrome +
Alstrom syndrome
Alstrom syndrome
amelogenesis imperfecta hypomaturation type 2A2
amelogenesis imperfecta hypomaturation type 2A3
amelogenesis imperfecta hypomaturation type 2A4
amelogenesis imperfecta hypomaturation type 2A5
amelogenesis imperfecta type 1C
amelogenesis imperfecta type 1F
amelogenesis imperfecta type 1G
amelogenesis imperfecta type 1H
amelogenesis imperfecta type 2A1
Angelman syndrome
anterior segment dysgenesis 2
anterior segment dysgenesis 7
anterior segment dysgenesis 8
anterior spinal artery syndrome
Antley-Bixler syndrome
Antley-Bixler syndrome
aplasia of lacrimal and salivary glands
ARC syndrome +
ARC syndrome +
arrhythmogenic right ventricular dysplasia 11
asphyxiating thoracic dystrophy +
Athabaskan brainstem dysgenesis syndrome
atransferrinemia
atrichia with papular lesions
autoimmune lymphoproliferative syndrome type 2B
autoimmune lymphoproliferative syndrome type 3
autosomal dominant keratitis-ichthyosis-deafness syndrome
autosomal recessive Alport syndrome
autosomal recessive centronuclear myopathy +
autosomal recessive cerebellar ataxia +
autosomal recessive chronic granulomatous disease cytochrome b-negative
autosomal recessive chronic granulomatous disease cytochrome b-positive type I
autosomal recessive chronic granulomatous disease cytochrome b-positive type II
autosomal recessive chronic granulomatous disease cytochrome b-positive type III
autosomal recessive congenital ichthyosis +
autosomal recessive cutis laxa type I +
autosomal recessive cutis laxa type II classic type +
autosomal recessive cutis laxa type IIB
autosomal recessive cutis laxa type III +
autosomal recessive distal hereditary motor neuronopathy +
autosomal recessive dyskeratosis congenita 1
autosomal recessive dyskeratosis congenita 2
autosomal recessive dyskeratosis congenita 3
autosomal recessive dyskeratosis congenita 4
autosomal recessive dyskeratosis congenita 5
autosomal recessive dyskeratosis congenita 6
autosomal recessive Emery-Dreifuss muscular dystrophy 3
autosomal recessive hyaline body myopathy
autosomal recessive hypophosphatemic rickets
autosomal recessive isolated ectopia lentis 2
autosomal recessive non-syndromic intellectual disability +
autosomal recessive nonsyndromic deafness +
autosomal recessive osteopetrosis 1
autosomal recessive osteopetrosis 2
autosomal recessive osteopetrosis 3
autosomal recessive osteopetrosis 4
autosomal recessive osteopetrosis 5
autosomal recessive osteopetrosis 6
autosomal recessive osteopetrosis 7
autosomal recessive osteopetrosis 8
autosomal recessive pericentral pigmentary retinopathy
autosomal recessive polycystic kidney disease +
autosomal recessive progressive external ophthalmoplegia 1
autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 2
autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 3
autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 4
autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 5
autosomal recessive pseudohypoaldosteronism type 1
autosomal recessive pyridoxine-refractory sideroblastic anemia 2
autosomal recessive pyridoxine-refractory sideroblastic anemia 3
autosomal recessive Robinow syndrome
autosomal recessive type IV Ehlers-Danlos syndrome
autosomal recessive Whistling face syndrome
autosomal recessive woolly hair 3
Ayme-Gripp syndrome
Bannayan-Riley-Ruvalcaba syndrome
Baraitser-Winter syndrome
Barber-Say syndrome
Bardet-Biedl syndrome +
Bardet-Biedl syndrome +
Barre-Lieou syndrome
Bart-Pumphrey syndrome
basilar artery insufficiency
Beare-Stevenson cutis gyrata syndrome
Beckwith-Wiedemann syndrome
Beemer-Langer syndrome
Behr syndrome
benign recurrent intrahepatic cholestasis 1
benign recurrent intrahepatic cholestasis 2
beta-ketothiolase deficiency
Birk-Barel syndrome
Bjornstad syndrome
Bjornstad syndrome
Blau syndrome
blepharocheilodontic syndrome +
blepharophimosis, ptosis, and epicanthus inversus syndrome
Bloom syndrome
Bloom syndrome
Boucher-Neuhauser syndrome
Boucher-Neuhauser syndrome
Bowen-Conradi syndrome
Bowen-Conradi syndrome
brachydactyly-syndactyly syndrome
brachyolmia-amelogenesis imperfecta syndrome
brachyolmia-amelogenesis imperfecta syndrome
branched-chain keto acid dehydrogenase kinase deficiency
branchiooculofacial syndrome
branchiootic syndrome
branchiootorenal syndrome +
Brown-Vialetto-Van Laere syndrome
Brown-Vialetto-Van Laere syndrome
Bruck syndrome
Buschke-Ollendorff syndrome
C syndrome
camptodactyly-arthropathy-coxa vara-pericarditis syndrome
camptodactyly-arthropathy-coxa vara-pericarditis syndrome
camptodactyly-tall stature-scoliosis-hearing loss syndrome
Canavan disease
carbamoyl phosphate synthetase I deficiency disease
carboxypeptidase N deficiency
cardiofaciocutaneous syndrome +
Carey-Fineman-Ziter syndrome
Carney complex
Carney-Stratakis syndrome
carnitine-acylcarnitine translocase deficiency
cartilage-hair hypoplasia
Cauda equina syndrome
CD3epsilon deficiency
CD3gamma deficiency
CEDNIK syndrome
CEDNIK syndrome
cerebrocostomandibular syndrome
Charcot-Marie-Tooth disease axonal type 2H
Charcot-Marie-Tooth disease axonal type 2K
Charcot-Marie-Tooth disease axonal type 2P
Charcot-Marie-Tooth disease axonal type 2S
Charcot-Marie-Tooth disease axonal type 2T
Charcot-Marie-Tooth disease axonal type 2X
Charcot-Marie-Tooth disease recessive intermediate A
Charcot-Marie-Tooth disease recessive intermediate B
Charcot-Marie-Tooth disease recessive intermediate C
Charcot-Marie-Tooth disease recessive intermediate D
Charcot-Marie-Tooth disease type 1F
Charcot-Marie-Tooth disease type 2A2B
Charcot-Marie-Tooth disease type 2B1
Charcot-Marie-Tooth disease type 2B2
Charcot-Marie-Tooth disease type 2EE
Charcot-Marie-Tooth disease type 2R
Charcot-Marie-Tooth disease type 3
Charcot-Marie-Tooth disease type 4A
Charcot-Marie-Tooth disease type 4B1
Charcot-Marie-Tooth disease type 4B2
Charcot-Marie-Tooth disease type 4B3
Charcot-Marie-Tooth disease type 4C
Charcot-Marie-Tooth disease type 4D
Charcot-Marie-Tooth disease type 4E
Charcot-Marie-Tooth disease type 4F
Charcot-Marie-Tooth disease type 4G
Charcot-Marie-Tooth disease type 4H
Charcot-Marie-Tooth disease type 4J
Charcot-Marie-Tooth disease type 4K
CHARGE syndrome
Chediak-Higashi syndrome
Chediak-Higashi syndrome
chondrodysplasia punctata +
chondrodysplasia-pseudohermaphroditism syndrome
choreaacanthocytosis
chronic atrial and intestinal dysrhythmia
chronic fatigue syndrome
ciliopathy +
classic galactosemia
cleft lip-palate-ectodermal dysplasia syndrome
cleft lip-palate-ectodermal dysplasia syndrome
CLOVES syndrome
COACH syndrome
COACH syndrome
Cockayne syndrome
Cockayne syndrome
cocoon syndrome
cocoon syndrome
CODAS syndrome
CODAS syndrome
Coffin-Lowry syndrome
Coffin-Siris syndrome +
Cohen syndrome
Cohen syndrome
cold-induced sweating syndrome +
cold-induced sweating syndrome +
combined D-2- and L-2-hydroxyglutaric aciduria
combined malonic and methylmalonic acidemia
combined oxidative phosphorylation deficiency 1
combined oxidative phosphorylation deficiency 10
combined oxidative phosphorylation deficiency 11
combined oxidative phosphorylation deficiency 12
combined oxidative phosphorylation deficiency 13
combined oxidative phosphorylation deficiency 14
combined oxidative phosphorylation deficiency 15
combined oxidative phosphorylation deficiency 16
combined oxidative phosphorylation deficiency 17
combined oxidative phosphorylation deficiency 18
combined oxidative phosphorylation deficiency 19
combined oxidative phosphorylation deficiency 2
combined oxidative phosphorylation deficiency 20
combined oxidative phosphorylation deficiency 21
combined oxidative phosphorylation deficiency 22
combined oxidative phosphorylation deficiency 23
combined oxidative phosphorylation deficiency 24
combined oxidative phosphorylation deficiency 25
combined oxidative phosphorylation deficiency 26
combined oxidative phosphorylation deficiency 27
combined oxidative phosphorylation deficiency 28
combined oxidative phosphorylation deficiency 29
combined oxidative phosphorylation deficiency 3
combined oxidative phosphorylation deficiency 30
combined oxidative phosphorylation deficiency 31
combined oxidative phosphorylation deficiency 32
combined oxidative phosphorylation deficiency 33
combined oxidative phosphorylation deficiency 34
combined oxidative phosphorylation deficiency 35
combined oxidative phosphorylation deficiency 36
combined oxidative phosphorylation deficiency 37
combined oxidative phosphorylation deficiency 38
combined oxidative phosphorylation deficiency 39
combined oxidative phosphorylation deficiency 4
combined oxidative phosphorylation deficiency 5
combined oxidative phosphorylation deficiency 7
combined oxidative phosphorylation deficiency 8
combined oxidative phosphorylation deficiency 9
congenital adrenal insufficiency
congenital amegakaryocytic thrombocytopenia
congenital diarrhea 5 with tufting enteropathy
congenital diarrhea 7 with exudative enteropathy
congenital disorder of glycosylation Ia
congenital disorder of glycosylation Iaa
congenital disorder of glycosylation Ib
congenital disorder of glycosylation Ic
congenital disorder of glycosylation Id
congenital disorder of glycosylation Ie
congenital disorder of glycosylation If
congenital disorder of glycosylation Ig
congenital disorder of glycosylation Ih
congenital disorder of glycosylation Ii
congenital disorder of glycosylation Ij
congenital disorder of glycosylation Ik
congenital disorder of glycosylation Il
congenital disorder of glycosylation Im
congenital disorder of glycosylation In
congenital disorder of glycosylation Ip
congenital disorder of glycosylation Iq
congenital disorder of glycosylation Ir
congenital disorder of glycosylation It
congenital disorder of glycosylation Iu
congenital disorder of glycosylation Iw
congenital disorder of glycosylation Ix
congenital disorder of glycosylation type IIa
congenital disorder of glycosylation type IIb
congenital disorder of glycosylation type IIc
congenital disorder of glycosylation type IId
congenital disorder of glycosylation type IIe
congenital disorder of glycosylation type IIf
congenital disorder of glycosylation type IIg
congenital disorder of glycosylation type IIh
congenital disorder of glycosylation type IIi
congenital disorder of glycosylation type IIj
congenital disorder of glycosylation type IIk
congenital disorder of glycosylation type IIl
congenital disorder of glycosylation type IIn
congenital disorder of glycosylation type IIo
congenital disorder of glycosylation type IIp
congenital disorder of glycosylation type IIq
congenital dyserythropoietic anemia type Ia
congenital dyserythropoietic anemia type Ib
congenital dyserythropoietic anemia type II
congenital generalized lipodystrophy +
congenital heart defects, hamartomas of tongue, and polysyndactyly
congenital heart defects, hamartomas of tongue, and polysyndactyly
congenital hereditary endothelial dystrophy of cornea
congenital hypotrichosis with juvenile macular dystrophy
congenital lactase deficiency
congenital leptin deficiency
congenital leptin deficiency
congenital malabsorptive diarrhea 4
congenital merosin-deficient muscular dystrophy 1A
congenital muscular dystrophy 1B
congenital muscular dystrophy due to integrin alpha-7 deficiency
congenital muscular dystrophy merosin-positive
congenital muscular dystrophy with cataracts and intellectual disability
congenital myasthenic syndrome 10
congenital myasthenic syndrome 11
congenital myasthenic syndrome 12
congenital myasthenic syndrome 13
congenital myasthenic syndrome 14
congenital myasthenic syndrome 15
congenital myasthenic syndrome 16
congenital myasthenic syndrome 17
congenital myasthenic syndrome 19
congenital myasthenic syndrome 1B
congenital myasthenic syndrome 20
congenital myasthenic syndrome 21
congenital myasthenic syndrome 22
congenital myasthenic syndrome 2C
congenital myasthenic syndrome 3B
congenital myasthenic syndrome 3C
congenital myasthenic syndrome 4A
congenital myasthenic syndrome 4B
congenital myasthenic syndrome 4C
congenital myasthenic syndrome 5
congenital myasthenic syndrome 6
congenital myasthenic syndrome 8
congenital myasthenic syndrome 9
congenital nongoitrous hypothyroidism 1
congenital nongoitrous hypothyroidism 4
congenital secretory chloride diarrhea 1
congenital secretory sodium diarrhea 3
congenital secretory sodium diarrhea 8
congenital stationary night blindness 1B
congenital stationary night blindness 1C
congenital stationary night blindness 1D
congenital stationary night blindness 1E
congenital stationary night blindness 1F
congenital stationary night blindness 1G
congenital stationary night blindness 1H
congenital sucrase-isomaltase deficiency
corneal dystrophy-perceptive deafness syndrome
corneal dystrophy-perceptive deafness syndrome
Cornelia de Lange syndrome +
cortical dysplasia-focal epilepsy syndrome
cortisone reductase deficiency 1
Costello syndrome
Cowden syndrome
craniofacial-deafness-hand syndrome
craniofrontonasal syndrome
craniolenticulosutural dysplasia
craniolenticulosutural dysplasia
CREST syndrome
Crouzon syndrome-acanthosis nigricans syndrome
Culler-Jones syndrome
Currarino syndrome
cystathioninuria
cystic fibrosis
cystic fibrosis
cystinosis
D-2-hydroxyglutaric aciduria 1
D-glyceric aciduria
Denys-Drash syndrome
diastrophic dysplasia
diffuse infiltrative lymphocytosis syndrome
dihydropyrimidinase deficiency
dilated cardiomyopathy 1X
dilated cardiomyopathy 2A
dilated cardiomyopathy 2B
dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome
distal arthrogryposis type 5D
DNA ligase IV deficiency
dominant optic atrophy plus syndrome
Donnai-Barrow syndrome
Donnai-Barrow syndrome
Donohue syndrome
Donohue syndrome
DOORS syndrome
DOORS syndrome
Duane-radial ray syndrome
Dubowitz syndrome
Dyggve-Melchior-Clausen disease +
dysplastic nevus syndrome
dystonia 16
dystonia 27
dystonia 5
early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome
EAST syndrome
EAST syndrome
ectodermal dysplasia +
ectodermal dysplasia 10B
ectodermal dysplasia 11B
ectodermal dysplasia 13
ectodermal dysplasia 14
ectodermal dysplasia 15
ectodermal dysplasia 4
ectodermal dysplasia 5
ectodermal dysplasia 6
ectodermal dysplasia 7
ectodermal dysplasia 8
ectodermal dysplasia 9
ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome
ectopia lentis with ectopia of pupil
EEC syndrome +
Ehlers-Danlos syndrome progeroid type
Ellis-Van Creveld syndrome
Ellis-Van Creveld syndrome
endocrine-cerebro-osteodysplasia syndrome
endocrine-cerebro-osteodysplasia syndrome
enhanced S-cone syndrome
enterokinase deficiency
epidermodysplasia verruciformis
erythrokeratodermia variabilis et progressiva 1
erythrokeratodermia variabilis et progressiva 4
erythrokeratodermia variabilis et progressiva 5
essential fructosuria
factor XII deficiency
familial adenomatous polyposis 2
familial adenomatous polyposis 3
familial adenomatous polyposis 4
familial adult myoclonic epilepsy 5
familial apolipoprotein C-II deficiency
familial benign fleck retina
familial erythrocytosis 2
familial GPIHBP1 deficiency
familial hemophagocytic lymphohistiocytosis 1
familial hemophagocytic lymphohistiocytosis 2
familial hemophagocytic lymphohistiocytosis 3
familial hemophagocytic lymphohistiocytosis 4
familial hepatic adenoma
familial isolated trichomegaly
familial lipase maturation factor 1 deficiency
familial lipoprotein lipase deficiency
familial partial lipodystrophy type 5
familial partial lipodystrophy type 6
familial temporal lobe epilepsy 5
Fanconi anemia complementation group A
Fanconi anemia complementation group C
Fanconi anemia complementation group D1
Fanconi anemia complementation group D2
Fanconi anemia complementation group E
Fanconi anemia complementation group I
Fanconi anemia complementation group L
Fanconi anemia complementation group O
Fanconi anemia complementation group P
Fanconi anemia complementation group Q
Fanconi anemia complementation group T
Fanconi anemia complementation group U
Fanconi anemia complementation group V
Fanconi-like syndrome
fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 1
fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 2
fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 3
fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 4
fatal infantile hypertonic myofibrillar myopathy
Feingold syndrome
Felty's syndrome
fetal akinesia deformation sequence syndrome +
fetal akinesia deformation sequence syndrome 1
fetal akinesia deformation sequence syndrome 2
fetal akinesia deformation sequence syndrome 3
fetal akinesia deformation sequence syndrome 4
fetal valproate syndrome
FG syndrome
fibrogenesis imperfecta ossium
fibular hypoplasia and complex brachydactyly
Floating-Harbor syndrome
focal dermal hypoplasia
focal segmental glomerulosclerosis 6
focal segmental glomerulosclerosis 9
fragile X syndrome
Fraser syndrome +
Fraser syndrome +
Frasier syndrome
Fuchs' heterochromic uveitis
Fuhrmann syndrome
fumarase deficiency
galactose epimerase deficiency
Galloway-Mowat syndrome +
Galloway-Mowat syndrome +
gamma-glutamyl transpeptidase deficiency
Gamstorp-Wohlfart syndrome
gangliosidosis +
geroderma osteodysplasticum
geroderma osteodysplasticum
giant axonal neuropathy 1
Gillespie syndrome
Gitelman syndrome
glutamate formiminotransferase deficiency
glutamate-cysteine ligase deficiency
glutaric acidemia I
Goldberg-Shprintzen syndrome
Goldberg-Shprintzen syndrome
Goldenhar syndrome
Gordon Holmes syndrome
Gorham's disease
GRACILE syndrome
Greenberg dysplasia
Griscelli syndrome +
Guttmacher syndrome
Hallermann-Streiff syndrome
hand-foot-genital syndrome
hereditary arterial and articular multiple calcification syndrome
hereditary arterial and articular multiple calcification syndrome
hereditary breast ovarian cancer syndrome
hereditary desmoid disease
hereditary folate malabsorption
hereditary sensory and autonomic neuropathy type 2A
hereditary sensory and autonomic neuropathy type 2B
hereditary sensory and autonomic neuropathy type 5
hereditary sensory and autonomic neuropathy type 6
hereditary sensory and autonomic neuropathy type 8
hereditary sensory neuropathy type 2C
hereditary sensory neuropathy type 4
hereditary spastic paraplegia 11
hereditary spastic paraplegia 14
hereditary spastic paraplegia 15
hereditary spastic paraplegia 18
hereditary spastic paraplegia 23
hereditary spastic paraplegia 24
hereditary spastic paraplegia 25
hereditary spastic paraplegia 26
hereditary spastic paraplegia 27
hereditary spastic paraplegia 28
hereditary spastic paraplegia 30
hereditary spastic paraplegia 32
hereditary spastic paraplegia 35
hereditary spastic paraplegia 39
hereditary spastic paraplegia 43
hereditary spastic paraplegia 44
hereditary spastic paraplegia 45
hereditary spastic paraplegia 46
hereditary spastic paraplegia 47
hereditary spastic paraplegia 48
hereditary spastic paraplegia 49
hereditary spastic paraplegia 50
hereditary spastic paraplegia 51
hereditary spastic paraplegia 52
hereditary spastic paraplegia 53
hereditary spastic paraplegia 54
hereditary spastic paraplegia 55
hereditary spastic paraplegia 56
hereditary spastic paraplegia 57
hereditary spastic paraplegia 5A
hereditary spastic paraplegia 61
hereditary spastic paraplegia 62
hereditary spastic paraplegia 63
hereditary spastic paraplegia 64
hereditary spastic paraplegia 7
hereditary spastic paraplegia 72
hereditary spastic paraplegia 74
hereditary spastic paraplegia 75
hereditary spastic paraplegia 76
hereditary spastic paraplegia 77
hereditary spastic paraplegia 9A
hereditary spastic paraplegia 9B
hereditary spherocytosis type 1
hereditary spherocytosis type 3
hereditary spherocytosis type 5
Hermansky-Pudlak syndrome +
Hermansky-Pudlak syndrome +
high molecular weight kininogen deficiency
high myopia-sensorineural deafness syndrome
high myopia-sensorineural deafness syndrome
histiocytosis-lymphadenopathy plus syndrome
histiocytosis-lymphadenopathy plus syndrome
holoprosencephaly +
Holt-Oram syndrome
Holzgreve-Wagner-Rehder Syndrome
hyaline fibromatosis syndrome
hydrolethalus syndrome +
hydrolethalus syndrome +
hyper IgE recurrent infection syndrome 2
hyper IgE recurrent infection syndrome 3
hyper IgE recurrent infection syndrome 4
hyperekplexia 1
hyperekplexia 2
hyperekplexia 3
hyperekplexia 4
hyperferritinemia-cataract syndrome
hyperphosphatemic familial tumoral calcinosis
hyperprolinemia type 1
hyperprolinemia type 2
hypertelorism, microtia, facial clefting syndrome
hypertelorism, microtia, facial clefting syndrome
hypertension and brachydactyly syndrome
hypogonadotropic hypogonadism 10 with or without anosmia
hypogonadotropic hypogonadism 11 with or without anosmia
hypogonadotropic hypogonadism 12 with or without anosmia
hypogonadotropic hypogonadism 13 with or without anosmia
hypogonadotropic hypogonadism 18 with or without anosmia
hypogonadotropic hypogonadism 22 with or without anosmia
hypogonadotropic hypogonadism 23 with or without anosmia
hypogonadotropic hypogonadism 24 without anosmia
hypogonadotropic hypogonadism 7 with or without anosmia
hypogonadotropic hypogonadism 8 with or without anosmia
hypomyelinating leukodystrophy 10
hypomyelinating leukodystrophy 11
hypomyelinating leukodystrophy 12
hypomyelinating leukodystrophy 13
hypomyelinating leukodystrophy 14
hypomyelinating leukodystrophy 2
hypomyelinating leukodystrophy 3
hypomyelinating leukodystrophy 4
hypomyelinating leukodystrophy 5
hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism
hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism
hypomyelinating leukodystrophy 9
hypoparathyroidism-retardation-dysmorphism syndrome
hypoparathyroidism-retardation-dysmorphism syndrome
hypophosphatasia +
hypoplastic or aplastic tibia with polydactyly
hypotonia-cystinuria syndrome
hypotrichosis 10
hypotrichosis 6
hypotrichosis 7
hypotrichosis 8
hypotrichosis 9
hypotrichosis-lymphedema-telangiectasia syndrome
hypotrichosis-lymphedema-telangiectasia syndrome
hypotrichosis-lymphedema-telangiectasia-renal defect syndrome
IGSF1 deficiency syndrome
IMAGe syndrome
immunodeficiency with hyper IgM type 3
immunodeficiency with hyper IgM type 5
immunodeficiency with hyper-IgM type 2
immunodeficiency-centromeric instability-facial anomalies syndrome +
immunodeficiency-centromeric instability-facial anomalies syndrome +
immunoglobulin alpha deficiency
inclusion body myopathy with Paget disease of bone and frontotemporal dementia +
infantile cerebellar-retinal degeneration
infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
inflammatory bowel disease 25
inflammatory bowel disease 28
intellectual developmental disorder with short stature and behavioral abnormalities
intellectual developmental disorder with short stature and behavioral abnormalities
intermediate spinal muscular atrophy
irritable bowel syndrome
isolated hyperchlorhidrosis
isolated microphthalmia 1
isolated microphthalmia 2
isolated microphthalmia 3
isolated microphthalmia 5
isolated microphthalmia 6
isolated microphthalmia 8
isolated sulfite oxidase deficiency
IVIC syndrome
Jackson-Weiss syndrome
Jackson-Weiss syndrome
Jalili syndrome
Jalili syndrome
JMP syndrome
JMP syndrome
Johanson-Blizzard syndrome
Johanson-Blizzard syndrome
junctional epidermolysis bullosa Herlitz type
junctional epidermolysis bullosa non-Herlitz type
junctional epidermolysis bullosa with pyloric atresia
juvenile polyposis-hereditary hemorrhagic telangiectasia syndrome
Kabuki syndrome
Kahrizi syndrome
Kahrizi syndrome
karyomegalic interstitial nephritis
Kaufman oculocerebrofacial syndrome
KBG syndrome
Kleefstra syndrome +
Klippel-Feil syndrome +
Klippel-Feil syndrome 2
Klippel-Feil syndrome 4
Klippel-Trenaunay syndrome
Kohlschutter-Tonz syndrome
Kohlschutter-Tonz syndrome
Koolen de Vries syndrome
Kufor-Rakeb syndrome
LADD syndrome
Lafora disease
Laron syndrome
Laron syndrome
Larsen syndrome
Larsen-like syndrome B3GAT3 type
Larsen-like syndrome B3GAT3 type
late-adult onset retinitis pigmentosa
lateral meningocele syndrome
Laurence-Moon syndrome
Laurence-Moon syndrome
Leber congenital amaurosis 1
Leber congenital amaurosis 12
Leber congenital amaurosis 13
Leber congenital amaurosis 14
Leber congenital amaurosis 15
Leber congenital amaurosis 16
Leber congenital amaurosis 17
Leber congenital amaurosis 2
Leber congenital amaurosis 4
Leber congenital amaurosis 5
Leber congenital amaurosis 6
Leber congenital amaurosis 8
Leber congenital amaurosis 9
Lenz-Majewski hyperostotic dwarfism
LEOPARD syndrome +
lethal congenital contracture syndrome +
lethal congenital contracture syndrome +
lethal restrictive dermopathy
leukocyte adhesion deficiency +
Li-Fraumeni syndrome +
linear nevus sebaceous syndrome
Loeys-Dietz syndrome +
Lown-Ganong-Levine syndrome
lymphedema-distichiasis syndrome
lymphoproliferative syndrome 1
lymphoproliferative syndrome 2
Lynch syndrome +
macrocephaly-autism syndrome
Maffucci syndrome
mandibulofacial dysostosis with alopecia
mandibulofacial dysostosis, Guion-Almeida type
Marinesco-Sjogren syndrome
Marinesco-Sjogren syndrome
Marshall-Smith syndrome
Martsolf syndrome
Martsolf syndrome
Matthew-Wood syndrome
McCune Albright syndrome
McKusick-Kaufman syndrome
McKusick-Kaufman syndrome
median arcuate ligament syndrome
MEDNIK syndrome
megaconial type congenital muscular dystrophy
megacystis-microcolon-intestinal hypoperistalsis syndrome
megalencephalic leukoencephalopathy with subcortical cysts 1
megalencephalic leukoencephalopathy with subcortical cysts 2A
Meier-Gorlin syndrome +
Meier-Gorlin syndrome 1
Meier-Gorlin syndrome 2
Meier-Gorlin syndrome 3
Meier-Gorlin syndrome 4
Meier-Gorlin syndrome 5
Meier-Gorlin syndrome 7
Meier-Gorlin syndrome 8
melanoma and neural system tumor syndrome
microcephalic osteodysplastic primordial dwarfism type I
microcephalic osteodysplastic primordial dwarfism type II
microcephaly and chorioretinopathy 1
microcephaly and chorioretinopathy 1
microcephaly and chorioretinopathy 2
microcephaly and chorioretinopathy 2
microcephaly and chorioretinopathy 3
microcephaly and chorioretinopathy 3
microcephaly with or without chorioretinopathy, lymphedema, or mental retardation
microphthalmia with limb anomalies
microphthalmia with limb anomalies
microvillus inclusion disease
Miller-Dieker lissencephaly syndrome
mitochondrial DNA depletion syndrome 1
mitochondrial DNA depletion syndrome 11
mitochondrial DNA depletion syndrome 12b
mitochondrial DNA depletion syndrome 13
mitochondrial DNA depletion syndrome 15
mitochondrial DNA depletion syndrome 2
mitochondrial DNA depletion syndrome 3
mitochondrial DNA depletion syndrome 4a
mitochondrial DNA depletion syndrome 4b
mitochondrial DNA depletion syndrome 5
mitochondrial DNA depletion syndrome 6
mitochondrial DNA depletion syndrome 7
mitochondrial DNA depletion syndrome 8a
mitochondrial DNA depletion syndrome 8b
mitochondrial DNA depletion syndrome 9
mitochondrial pyruvate carrier deficiency
mitochondrial trifunctional protein deficiency
Miyoshi muscular dystrophy 1
Miyoshi muscular dystrophy 3
mosaic variegated aneuploidy syndrome 1
mosaic variegated aneuploidy syndrome 1
mosaic variegated aneuploidy syndrome 2
mosaic variegated aneuploidy syndrome 2
Mowat-Wilson syndrome
Muckle-Wells syndrome
mucopolysaccharidosis Ih
mucopolysaccharidosis Ih/s
mucopolysaccharidosis IVA
mucopolysaccharidosis type IIIA
mucopolysaccharidosis type IIIB
mucopolysaccharidosis type IIIC
mucopolysaccharidosis type IIID
mucopolysaccharidosis type IVB
mucosulfatidosis
mulibrey nanism
mulibrey nanism
multicentric carpotarsal osteolysis syndrome
multicentric reticulohistiocytosis
multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia and hydranencephaly
multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia and hydranencephaly
multiple chemical sensitivity
multiple congenital anomalies-hypotonia-seizures syndrome 1
multiple congenital anomalies-hypotonia-seizures syndrome 3
multiple endocrine neoplasia type 1
multiple endocrine neoplasia type 2A
multiple endocrine neoplasia type 2B
multiple endocrine neoplasia type 4
multiple epiphyseal dysplasia 4
multiple epiphyseal dysplasia 7
multiple epiphyseal dysplasia with myopia and deafness
multiple intestinal atresia
multiple mitochondrial dysfunctions syndrome 1
multiple mitochondrial dysfunctions syndrome 2
multiple mitochondrial dysfunctions syndrome 3
multiple mitochondrial dysfunctions syndrome 4
multiple mitochondrial dysfunctions syndrome 5
multiple mitochondrial dysfunctions syndrome 6
multiple pterygium syndrome
muscular dystrophy-dystroglycanopathy +
muscular dystrophy-dystroglycanopathy type B5
muscular dystrophy-dystroglycanopathy type B6
myofibrillar myopathy 1
myofibrillar myopathy 7
myofibrillar myopathy 8
myopathy with extrapyramidal signs
N syndrome
nail-patella syndrome
Nance-Horan syndrome
Nasu-Hakola disease
Nasu-Hakola disease
Native American myopathy
nemaline myopathy 1
nemaline myopathy 10
nemaline myopathy 11
nemaline myopathy 2
nemaline myopathy 3
nemaline myopathy 5
nemaline myopathy 7
nemaline myopathy 8
nemaline myopathy 9
neonatal diabetes mellitus with congenital hypothyroidism
nephronophthisis +
nephrotic syndrome type 1
nephrotic syndrome type 10
nephrotic syndrome type 11
nephrotic syndrome type 12
nephrotic syndrome type 13
nephrotic syndrome type 14
nephrotic syndrome type 15
nephrotic syndrome type 16
nephrotic syndrome type 17
nephrotic syndrome type 18
nephrotic syndrome type 19
nephrotic syndrome type 2
nephrotic syndrome type 3
nephrotic syndrome type 5
nephrotic syndrome type 6
nephrotic syndrome type 7
nephrotic syndrome type 8
nephrotic syndrome type 9
Netherton syndrome
neurodegeneration with brain iron accumulation 2a
neurodegeneration with brain iron accumulation 2b
neurodegeneration with brain iron accumulation 4
neurodegeneration with brain iron accumulation 6
neurodevelopmental disorder with midbrain and hindbrain malformations
neurofibromatosis +
neurofibromatosis-Noonan syndrome
neurogenic arthrogryposis multiplex congenita
neurooculocardiogenitourinary syndrome
nevoid basal cell carcinoma syndrome
Nezelof syndrome
NGLY1-deficiency
Nijmegen breakage syndrome
Nijmegen breakage syndrome
nonphotosensitive trichothiodystrophy
nonphotosensitive trichothiodystrophy
Noonan syndrome +
Noonan syndrome 2
Norman-Roberts syndrome
Norrie disease
oculoauricular syndrome
oculocerebrorenal syndrome
oculocutaneous albinism +
oculocutaneous albinism +
oculodentodigital dysplasia
Ogden syndrome
Oguchi disease-1
Oguchi disease-2
Ohdo syndrome +
Oliver-McFarlane syndrome
Oliver-McFarlane syndrome
Ollier disease
Opitz-GBBB syndrome
optic atrophy 11
optic atrophy 6
optic atrophy 7
optic atrophy 9
orofacial cleft +
orofacial cleft 14
orofacial cleft 7
orofaciodigital syndrome +
orofaciodigital syndrome V
osteogenesis imperfecta type 10
osteogenesis imperfecta type 11
osteogenesis imperfecta type 12
osteogenesis imperfecta type 13
osteogenesis imperfecta type 15
osteogenesis imperfecta type 17
osteogenesis imperfecta type 7
osteogenesis imperfecta type 8
osteogenesis imperfecta type 9
osteoporosis-pseudoglioma syndrome
osteoporosis-pseudoglioma syndrome
otulipenia
ovarian dysgenesis 1
ovarian dysgenesis 3
ovarian dysgenesis 4
ovarian dysgenesis 5
ovarian dysgenesis 6
ovarian dysgenesis 7
pachyonychia congenita
palindromic rheumatism
Pallister-Hall syndrome
palmoplantar keratoderma-deafness syndrome
palmoplantar keratoderma-esophageal carcinoma syndrome
pantothenate kinase-associated neurodegeneration
PAPA syndrome
Papillon-Lefevre disease
Parkinson's disease 14
Parkinson's disease 15
Parkinson's disease 19A
Parkinson's disease 2
Parkinson's disease 20
Parkinson's disease 23
Parkinson's disease 6
Parkinson's disease 7
PCWH syndrome
Pendred Syndrome
Pendred Syndrome
pentosuria
Perlman syndrome
permanent neonatal diabetes mellitus
Perrault syndrome +
Perrault syndrome +
Perry syndrome
persian gulf syndrome
Peters plus syndrome
PHARC syndrome
PHARC syndrome
photosensitive trichothiodystrophy
Pierson syndrome
Pierson syndrome
Pitt-Hopkins syndrome
Pitt-Hopkins-like syndrome 2
plasminogen deficiency type I
plasminogen deficiency type I
poikiloderma with neutropenia
polycystic ovary syndrome
popliteal pterygium syndrome
post-cardiac arrest syndrome
postaxial acrofacial dysostosis
postaxial acrofacial dysostosis
Potocki-Shaffer syndrome
Prader-Willi syndrome
primary autosomal recessive microcephaly +
primary hypertrophic osteoarthropathy
progeria
progressive familial intrahepatic cholestasis 1
progressive familial intrahepatic cholestasis 2
progressive familial intrahepatic cholestasis 3
progressive familial intrahepatic cholestasis 4
progressive familial intrahepatic cholestasis 5
progressive myoclonus epilepsy 10
progressive myoclonus epilepsy 1A
progressive myoclonus epilepsy 1B
progressive myoclonus epilepsy 3
progressive myoclonus epilepsy 4
progressive myoclonus epilepsy 6
progressive myoclonus epilepsy 8
progressive myoclonus epilepsy 9
progressive osseous heteroplasia
progressive pseudorheumatoid arthropathy of childhood
prolidase deficiency
proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome
proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome
Proteus syndrome
prothrombin deficiency
proximal symphalangism
prune belly syndrome
prune belly syndrome
pseudo-TORCH syndrome 1
pseudo-TORCH syndrome 1
pseudoxanthoma elasticum
psoriatic arthritis
PTEN hamartoma tumor syndrome
purine nucleoside phosphorylase deficiency
pycnodysostosis
pyruvate kinase deficiency of red cells
Qazi Markouizos syndrome
rapadilino syndrome
rapadilino syndrome
recessive dystrophic epidermolysis bullosa
renal coloboma syndrome
reticular dysgenesis
retinitis pigmentosa 1
retinitis pigmentosa 12
retinitis pigmentosa 14
retinitis pigmentosa 19
retinitis pigmentosa 20
retinitis pigmentosa 25
retinitis pigmentosa 26
retinitis pigmentosa 28
retinitis pigmentosa 29
retinitis pigmentosa 35
retinitis pigmentosa 37
retinitis pigmentosa 38
retinitis pigmentosa 4
retinitis pigmentosa 40
retinitis pigmentosa 41
retinitis pigmentosa 45
retinitis pigmentosa 50
retinitis pigmentosa 56
retinitis pigmentosa 57
retinitis pigmentosa 59
retinitis pigmentosa 62
retinitis pigmentosa 68
retinitis pigmentosa 69
retinitis pigmentosa 7
retinitis pigmentosa 71
retinitis pigmentosa 72
retinitis pigmentosa 73
retinitis pigmentosa 74
retinitis pigmentosa 75
retinitis pigmentosa 77
retinitis pigmentosa with or without situs inversus
Reye syndrome
rhizomelic chondrodysplasia punctata +
RIDDLE syndrome
RIDDLE syndrome
right atrial isomerism
rigid spine muscular dystrophy 1
Ritscher-Schinzel syndrome +
Ritscher-Schinzel syndrome 1
Roberts syndrome
Roberts syndrome
Robinow syndrome +
Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome
Rubinstein-Taybi syndrome
Ruijs-Aalfs syndrome
Ruijs-Aalfs syndrome
SADDAN
Saldino-Noonan syndrome
Saldino-Noonan syndrome
salt and pepper syndrome
salt and pepper syndrome
SAPHO syndrome
SC phocomelia syndrome
SC phocomelia syndrome
Schimke immuno-osseous dysplasia
Schwartz-Jampel syndrome 1
Schwartz-Jampel syndrome 1
sclerosteosis 1
sclerosteosis 2
Seckel syndrome +
Seckel syndrome +
Sengers syndrome
Senior-Loken syndrome
Senior-Loken syndrome
Sensenbrenner syndrome
Sensenbrenner syndrome
sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
sepiapterin reductase deficiency
septooptic dysplasia
severe combined immunodeficiency with sensitivity to ionizing radiation
severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, Nk cell-positive
severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive
SHORT syndrome
Shwachman-Diamond syndrome
sickle cell anemia
sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay
Silverman-Handmaker type dyssegmental dysplasia
Simpson-Golabi-Behmel syndrome type 1
Simpson-Golabi-Behmel syndrome type 2
sitosterolemia
Sjogren-Larsson syndrome
Sjogren-Larsson syndrome
SOST-related sclerosing bone dysplasia
Sotos syndrome
Sotos syndrome
spermatogenic failure 13
spermatogenic failure 14
spermatogenic failure 15
spermatogenic failure 16
spermatogenic failure 17
spermatogenic failure 18
spermatogenic failure 19
spermatogenic failure 20
spermatogenic failure 21
spermatogenic failure 22
spermatogenic failure 23
spermatogenic failure 5
spermatogenic failure 6
spermatogenic failure 7
spermatogenic failure 9
spinal muscular atrophy with progressive myoclonic epilepsy
spinocerebellar ataxia type 1 with axonal neuropathy
split hand-foot malformation 1 with sensorineural hearing loss
split hand-foot malformation 6
SPOAN syndrome
spondylocarpotarsal synostosis syndrome
spondyloepimetaphyseal dysplasia, Genevieve-type
spondyloepimetaphyseal dysplasia, Pakistani type
spondyloepimetaphyseal dysplasia, Sponastrime type
Stickler syndrome
subclavian steal syndrome
sudden infant death syndrome
Sweeney-Cox syndrome
T-cell immunodeficiency, congenital alopecia, and nail dystrophy
Takayasu's arteritis
temtamy preaxial brachydactyly syndrome
temtamy preaxial brachydactyly syndrome
Temtamy syndrome
Temtamy syndrome
thalassemia +
thiamine-responsive megaloblastic anemia syndrome
thiamine-responsive megaloblastic anemia syndrome
Tietz syndrome
Tietze's syndrome
Timothy syndrome
tooth and nail syndrome
torsion dystonia 17
torsion dystonia 2
Townes-Brocks syndrome
transient bullous dermolysis of the newborn
Treacher Collins syndrome
trichodontoosseous syndrome
trichohepatoenteric syndrome +
trichohepatoenteric syndrome +
trichorhinophalangeal syndrome type I
trichorhinophalangeal syndrome type II
trichorhinophalangeal syndrome type III
trimethylaminuria
triple-A syndrome
triple-A syndrome
Troyer syndrome
tuberous sclerosis +
Ullrich congenital muscular dystrophy
ulnar-mammary syndrome
urofacial syndrome
urofacial syndrome
Usher syndrome +
Usher syndrome +
UV-sensitive syndrome
uveal coloboma-cleft lip and palate-intellectual disability
VACTERL association
Van der Woude syndrome
Van Maldergem syndrome +
Van Maldergem syndrome +
ventriculomegaly - cystic kidney disease
ventriculomegaly - cystic kidney disease
vertebral artery insufficiency
Vici syndrome
Vici syndrome
Vohwinkel syndrome
Waardenburg's syndrome +
Walker-Warburg syndrome
Warburg micro syndrome +
Warburg micro syndrome +
Warsaw breakage syndrome
Warsaw breakage syndrome
Weaver syndrome
Weill-Marchesani syndrome
Werner syndrome
Werner syndrome
Wiskott-Aldrich syndrome
Wissler's syndrome
Wolcott-Rallison syndrome
Wolcott-Rallison syndrome
Wolfram syndrome +
Wolfram syndrome 1
Wolfram syndrome 2
xeroderma pigmentosum +
xeroderma pigmentosum +
XFE progeroid syndrome
XFE progeroid syndrome
yellow nail syndrome
Yunis-Varon syndrome
Yunis-Varon syndrome
Zika virus congenital syndrome
Zollinger-Ellison syndrome
Child term(s)

is-a denotes an 'is-a' relationship