Term with siblings
DiGeorge syndrome

3-M syndrome
3MC syndrome +
3p deletion syndrome
46,XX sex reversal 2
46,XX sex reversal 4
46,XY sex reversal 10
46,XY sex reversal 3
46,XY sex reversal 6
46,XY sex reversal 9
Aagenaes syndrome
Aarskog syndrome +
ABCD syndrome
abdominal obesity-metabolic syndrome +
abdominal obesity-metabolic syndrome +
ablepharon macrostomia syndrome
ablepharon macrostomia syndrome
Abruzzo-Erickson syndrome
achalasia microcephaly syndrome
Achard syndrome
achondrogenesis type II
acrocallosal syndrome
acrofacial dysostosis Cincinnati type
acrokeratosis verruciformis
acrorenal syndrome
Adams-Oliver syndrome
adermatoglyphia
Adie syndrome
ADULT syndrome
ADULT syndrome
adult-onset autosomal dominant demyelinating leukodystrophy
adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
advanced sleep phase syndrome +
agammaglobulinemia 5
age related macular degeneration +
Aicardi syndrome
Aicardi-Goutieres syndrome
Alexander disease
Alkuraya-Kucinskas syndrome
Allan-Herndon-Dudley syndrome
alopecia-mental retardation syndrome +
Alport syndrome +
Alstrom syndrome
Alzheimer's disease 1
Alzheimer's disease 2
Alzheimer's disease 3
Alzheimer's disease 4
Alzheimer's disease 5
Alzheimer's disease 9
amelogenesis imperfecta type 1A
amelogenesis imperfecta type 1B
amelogenesis imperfecta type 3A
amelogenesis imperfecta type 3B
amelogenesis imperfecta type 4
AMME complex
Andersen-Tawil syndrome
Angelman syndrome
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
ankylosing spondylitis 2
ankyrin-B-related cardiac arrhythmia
anterior segment dysgenesis 1
anterior segment dysgenesis 3
anterior segment dysgenesis 4
anterior spinal artery syndrome
antithrombin III deficiency
Antley-Bixler syndrome
aplasia of lacrimal and salivary glands
aplasia of lacrimal and salivary glands
apolipoprotein C-III deficiency
APP-related cerebral amyloid angiopathy
ARC syndrome +
arrhythmogenic right ventricular dysplasia 1
arrhythmogenic right ventricular dysplasia 10
arrhythmogenic right ventricular dysplasia 11
arrhythmogenic right ventricular dysplasia 12
arrhythmogenic right ventricular dysplasia 13
arrhythmogenic right ventricular dysplasia 2
arrhythmogenic right ventricular dysplasia 3
arrhythmogenic right ventricular dysplasia 4
arrhythmogenic right ventricular dysplasia 5
arrhythmogenic right ventricular dysplasia 8
arrhythmogenic right ventricular dysplasia 9
atrial heart septal defect 2
atrial heart septal defect 5
atrial heart septal defect 6
atrial heart septal defect 7
atrial heart septal defect 8
atrial heart septal defect 9
atrial standstill 1
autoimmune lymphoproliferative syndrome type 2A
autoimmune lymphoproliferative syndrome type 4
autosomal dominant beta thalassemia
autosomal dominant Aarskog syndrome
autosomal dominant Alport syndrome
autosomal dominant centronuclear myopathy +
autosomal dominant cerebellar ataxia +
autosomal dominant chondrodysplasia punctata
autosomal dominant congenital deafness with onychodystrophy
autosomal dominant congenital deafness with onychodystrophy
autosomal dominant cutis laxa +
autosomal dominant distal hereditary motor neuronopathy +
autosomal dominant dyskeratosis congenita 1
autosomal dominant dyskeratosis congenita 2
autosomal dominant dyskeratosis congenita 3
autosomal dominant dyskeratosis congenita 4
autosomal dominant dyskeratosis congenita 6
autosomal dominant Emery-Dreifuss muscular dystrophy 2
autosomal dominant Emery-Dreifuss muscular dystrophy 4
autosomal dominant Emery-Dreifuss muscular dystrophy 5
autosomal dominant Emery-Dreifuss muscular dystrophy 7
autosomal dominant familial periodic fever
autosomal dominant familial visceral neuropathy
autosomal dominant hyaline body myopathy
autosomal dominant hypocalcemia +
autosomal dominant hypophosphatemic rickets
autosomal dominant isolated ectopia lentis 1
autosomal dominant keratitis
autosomal dominant keratitis-ichthyosis-deafness syndrome
autosomal dominant keratitis-ichthyosis-deafness syndrome
autosomal dominant limb-girdle muscular dystrophy +
autosomal dominant macrothrombocytopenia TUBB1-related
autosomal dominant mental retardation 55
autosomal dominant mental retardation 56
autosomal dominant microcephaly
autosomal dominant mutilating palmoplantar keratoderma with periorificial keratotic plaques
autosomal dominant nocturnal frontal lobe epilepsy +
autosomal dominant non-syndromic intellectual disability +
autosomal dominant nonsyndromic deafness +
autosomal dominant osteopetrosis 1
autosomal dominant osteopetrosis 2
autosomal dominant polycystic kidney disease +
autosomal dominant progressive external ophthalmoplegia 1
autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6
autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2
autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3
autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4
autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5
autosomal dominant pseudohypoaldosteronism type 1
autosomal dominant Robinow syndrome 1
autosomal dominant Robinow syndrome 2
autosomal dominant Robinow syndrome 3
autosomal dominant sensory ataxia 1
autosomal dominant sideroblastic anemia 4
autosomal dominant thrombophilia due to protein S deficiency
autosomal dominant vitreoretinochoroidopathy
autosomal dominant Wolfram syndrome
autosomal dominant woolly hair
Axenfeld-Rieger syndrome +
Ayme-Gripp syndrome
Ayme-Gripp syndrome
Bannayan-Riley-Ruvalcaba syndrome
Bannayan-Riley-Ruvalcaba syndrome
Baraitser-Winter syndrome
Barber-Say syndrome
Bardet-Biedl syndrome +
Barre-Lieou syndrome
Bart-Pumphrey syndrome
Bart-Pumphrey syndrome
basilar artery insufficiency
Beare-Stevenson cutis gyrata syndrome
Beare-Stevenson cutis gyrata syndrome
Beckwith-Wiedemann syndrome
Beemer-Langer syndrome
benign familial hematuria
Beukes hip dysplasia
bilateral optic nerve hypoplasia
Birk-Barel syndrome
Birk-Barel syndrome
Birt-Hogg-Dube syndrome
Bjornstad syndrome
Blau syndrome
Blau syndrome
blepharocheilodontic syndrome +
blepharocheilodontic syndrome +
blepharophimosis, ptosis, and epicanthus inversus syndrome
Bloom syndrome
blue color blindness
Bothnian type palmoplantar keratoderma
Boucher-Neuhauser syndrome
Bowen-Conradi syndrome
brachydactyly type A1 +
brachydactyly type A2
brachydactyly type C
brachydactyly type D
brachydactyly-syndactyly syndrome
brachydactyly-syndactyly syndrome
brachyolmia-amelogenesis imperfecta syndrome
branchiooculofacial syndrome
branchiooculofacial syndrome
branchiootic syndrome
branchiootorenal syndrome +
branchiootorenal syndrome +
bronchiectasis 1
bronchiectasis 2
bronchiectasis 3
Brooke-Spiegler syndrome
Brown-Vialetto-Van Laere syndrome
Bruck syndrome
Brugada syndrome 1
Brugada syndrome 7
Brugada syndrome 9
bullous congenital ichthyosiform erythroderma
Burn-McKeown syndrome
Buschke-Ollendorff syndrome
Buschke-Ollendorff syndrome
C syndrome
C syndrome
CADASIL 1
CADASIL 2
campomelic dysplasia
camptodactyly-arthropathy-coxa vara-pericarditis syndrome
camptodactyly-tall stature-scoliosis-hearing loss syndrome
cardiofaciocutaneous syndrome 1
cardiofaciocutaneous syndrome 2
cardiofaciocutaneous syndrome 3
cardiofaciocutaneous syndrome 4
Carey-Fineman-Ziter syndrome
Carney complex
Carney complex
Carney-Stratakis syndrome
Carney-Stratakis syndrome
cataract 47
Cauda equina syndrome
CEDNIK syndrome
cerebellar ataxia, mental retardation and dysequlibrium syndrome
cerebellar hyplasia/atrophy, epilepsy, and global developmental delay
cerebrocostomandibular syndrome
cerebrocostomandibular syndrome
Charcot-Marie-Tooth disease axonal type 2C
Charcot-Marie-Tooth disease axonal type 2CC
Charcot-Marie-Tooth disease axonal type 2F
Charcot-Marie-Tooth disease axonal type 2K
Charcot-Marie-Tooth disease axonal type 2L
Charcot-Marie-Tooth disease axonal type 2N
Charcot-Marie-Tooth disease axonal type 2O
Charcot-Marie-Tooth disease axonal type 2P
Charcot-Marie-Tooth disease axonal type 2Q
Charcot-Marie-Tooth disease axonal type 2T
Charcot-Marie-Tooth disease axonal type 2U
Charcot-Marie-Tooth disease axonal type 2V
Charcot-Marie-Tooth disease axonal type 2Z
Charcot-Marie-Tooth disease dominant intermediate A
Charcot-Marie-Tooth disease dominant intermediate B
Charcot-Marie-Tooth disease dominant intermediate C
Charcot-Marie-Tooth disease dominant intermediate D
Charcot-Marie-Tooth disease dominant intermediate E
Charcot-Marie-Tooth disease dominant intermediate F
Charcot-Marie-Tooth disease dominant intermediate G
Charcot-Marie-Tooth disease type 1A
Charcot-Marie-Tooth disease type 1B
Charcot-Marie-Tooth disease type 1C
Charcot-Marie-Tooth disease type 1D
Charcot-Marie-Tooth disease type 1E
Charcot-Marie-Tooth disease type 1F
Charcot-Marie-Tooth disease type 1G
Charcot-Marie-Tooth disease type 2A1
Charcot-Marie-Tooth disease type 2A2A
Charcot-Marie-Tooth disease type 2B
Charcot-Marie-Tooth disease type 2D
Charcot-Marie-Tooth disease type 2DD
Charcot-Marie-Tooth disease type 2E
Charcot-Marie-Tooth disease type 2I
Charcot-Marie-Tooth disease type 2J
Charcot-Marie-Tooth disease type 2Y
Charcot-Marie-Tooth disease type 3
Charcot-Marie-Tooth disease type 4E
Charcot-Marie-Tooth disease type 5
Charcot-Marie-Tooth disease, axonal type 2W
CHARGE syndrome
Chediak-Higashi syndrome
cherubism
CHILD syndrome
childhood onset GLUT1 deficiency syndrome 2
chondrodysplasia punctata +
chondrodysplasia-pseudohermaphroditism syndrome
chromosome 13q14 deletion syndrome
chromosome 15q11.2 deletion syndrome
chromosome 15q24 deletion syndrome
chromosome 15q25 deletion syndrome
chromosome 17p13.1 deletion syndrome
chromosome 17q11.2 deletion syndrome
chromosome 17q12 deletion syndrome
chromosome 18p deletion syndrome
chromosome 18q deletion syndrome
chromosome 19p13.13 deletion syndrome
chromosome 19q13.11 deletion syndrome
chromosome 5q12 deletion syndrome
chronic atrial and intestinal dysrhythmia
chronic fatigue syndrome
ciliopathy +
CINCA Syndrome
cleft lip-palate-ectodermal dysplasia syndrome
cleft palate, cardiac defects, and intellectual disabillity
cleft palate, cardiac defects, and intellectual disabillity
cleidocranial dysplasia
Clouston syndrome
CLOVES syndrome
COACH syndrome
Cockayne syndrome
CODAS syndrome
Coffin-Lowry syndrome
Coffin-Siris syndrome +
Cohen syndrome
COL4A1-related familial vascular leukoencephalopathy
cold-induced sweating syndrome +
complex cortical dysplasia with other brain malformations +
congenital adrenal insufficiency
congenital central hypoventilation syndrome
congenital contractural arachnodactyly
congenital diarrhea 6
congenital dyserythropoietic anemia type IV
congenital heart defects, hamartomas of tongue, and polysyndactyly
congenital leptin deficiency
congenital megabladder
congenital muscular dystrophy due to LMNA mutation
congenital myasthenic syndrome 18
congenital myasthenic syndrome 1A
congenital myasthenic syndrome 1B
congenital myasthenic syndrome 2A
congenital myasthenic syndrome 3A
congenital myasthenic syndrome 4A
congenital myasthenic syndrome 7
congenital nongoitrous hypothyroidism 2
congenital nongoitrous hypothyroidism 3
congenital nongoitrous hypothyroidism 5
congenital nongoitrous hypothyroidism 6
congenital nongoitrous hypothyroidism 8
congenital nystagmus 2
congenital nystagmus 3
congenital nystagmus 4
congenital nystagmus 7
congenital stationary night blindness autosomal dominant 1
congenital stationary night blindness autosomal dominant 2
congenital stationary night blindness autosomal dominant 3
congenital vertical talus
corneal dystrophy-perceptive deafness syndrome
Cornelia de Lange syndrome +
Cornelia de Lange syndrome 1
Cornelia de Lange syndrome 3
Cornelia de Lange syndrome 4
cortisone reductase deficiency 2
Costello syndrome
Cowden syndrome
Cowden syndrome
craniofacial-deafness-hand syndrome
craniofacial-deafness-hand syndrome
craniofrontonasal syndrome
craniolenticulosutural dysplasia
craniometaphyseal dysplasia
CREST syndrome
Cri-Du-Chat syndrome
Crouzon syndrome-acanthosis nigricans syndrome
Crouzon syndrome-acanthosis nigricans syndrome
CST3-related cerebral amyloid angiopathy
Culler-Jones syndrome
Culler-Jones syndrome
Currarino syndrome
Currarino syndrome
cystic fibrosis
D-2-hydroxyglutaric aciduria 2
dehydrated hereditary stomatocytosis 1
dehydrated hereditary stomatocytosis 2
delta beta-thalassemia
Denys-Drash syndrome
Denys-Drash syndrome
dermatopathia pigmentosa reticularis
dextro-looped transposition of the great arteries 1
dextro-looped transposition of the great arteries 3
Diamond Blackfan anemia 15 with mandibulofacial dysostosis
Diamond-Blackfan anemia 1
Diamond-Blackfan anemia 10
Diamond-Blackfan anemia 11
Diamond-Blackfan anemia 12
Diamond-Blackfan anemia 13
Diamond-Blackfan anemia 16
Diamond-Blackfan anemia 17
Diamond-Blackfan anemia 18
Diamond-Blackfan anemia 19
Diamond-Blackfan anemia 2
Diamond-Blackfan anemia 20
Diamond-blackfan anemia 3
Diamond-Blackfan anemia 4
Diamond-Blackfan anemia 5
Diamond-Blackfan anemia 6
Diamond-Blackfan anemia 7
Diamond-Blackfan anemia 8
Diamond-Blackfan anemia 9
diaphyseal medullary stenosis with malignant fibrous histiocytoma
diffuse cystic renal dysplasia
diffuse infiltrative lymphocytosis syndrome
dilated cardiomyopathy 1A
dilated cardiomyopathy 1AA
dilated cardiomyopathy 1B
dilated cardiomyopathy 1C
dilated cardiomyopathy 1CC
dilated cardiomyopathy 1D
dilated cardiomyopathy 1DD
dilated cardiomyopathy 1E
dilated cardiomyopathy 1HH
dilated cardiomyopathy 1II
dilated cardiomyopathy 1JJ
dilated cardiomyopathy 1KK
dilated cardiomyopathy 1NN
dilated cardiomyopathy 1R
dilated cardiomyopathy 1S
dilated cardiomyopathy 1U
dilated cardiomyopathy 1V
dilated cardiomyopathy 1Y
dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome
dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome
distal arthrogryposis type 10
distal arthrogryposis type 1A
distal arthrogryposis type 1B
distal arthrogryposis type 2A
distal arthrogryposis type 2B1
distal arthrogryposis type 2B2
distal arthrogryposis type 2B3
distal arthrogryposis type 3
distal arthrogryposis type 5
distal arthrogryposis type 7
distal myopathy 1
dominant optic atrophy plus syndrome
dominant optic atrophy plus syndrome
dominant pericentral pigmentary retinopathy
Donnai-Barrow syndrome
Donohue syndrome
DOORS syndrome
Doyne honeycomb retinal dystrophy
Duane-radial ray syndrome
Duane-radial ray syndrome
Dubowitz syndrome
dysplastic nevus syndrome
dysplastic nevus syndrome
dystonia 12
dystonia 21
dystonia 23
dystonia 24
dystonia 25
dystonia 5
dystonia 9
dystransthyretinemic hyperthyroxinemia
EAST syndrome
ectodermal dysplasia +
ectodermal dysplasia 10A
ectodermal dysplasia 11A
ectodermal dysplasia 12
EEC syndrome +
EEC syndrome +
Ehlers-Danlos syndrome arthrochalasia type 1
Ehlers-Danlos syndrome arthrochalasia type 2
Ehlers-Danlos syndrome classic type 1
Ehlers-Danlos syndrome classic type 2
Ellis-Van Creveld syndrome
Elsahy-Waters syndrome
encephalopathy due to defective mitochondrial and peroxisomal fission 1
endocrine-cerebro-osteodysplasia syndrome
epidermolysis bullosa simplex Dowling-Meara type
epidermolysis bullosa simplex generalized type
epidermolysis bullosa simplex localized type
epidermolysis bullosa simplex Ogna type
epidermolysis bullosa simplex with mottled pigmentation
epidermolysis bullosa simplex with muscular dystrophy
epidermolysis bullosa with congenital localized absence of skin and deformity of nails
episodic kinesigenic dyskinesia 1
episodic kinesigenic dyskinesia 2
epithelial basement membrane dystrophy
epithelial recurrent erosion dystrophy
erythrokeratodermia variabilis et progressiva 1
erythrokeratodermia variabilis et progressiva 2
erythrokeratodermia variabilis et progressiva 3
erythrokeratodermia variabilis et progressiva 6
essential tremor 1
essential tremor 2
essential tremor 4
essential tremor 5
exudative vitreoretinopathy 1
exudative vitreoretinopathy 3
exudative vitreoretinopathy 5
exudative vitreoretinopathy 6
exudative vitreoretinopathy 7
familial adenomatous polyposis 1
familial adult myoclonic epilepsy 1
familial adult myoclonic epilepsy 2
familial adult myoclonic epilepsy 3
familial adult myoclonic epilepsy 4
familial adult myoclonic epilepsy 6
familial adult myoclonic epilepsy 7
familial apolipoprotein A5 deficiency
familial cold autoinflammatory syndrome 1
familial cold autoinflammatory syndrome 2
familial cold autoinflammatory syndrome 3
familial cold autoinflammatory syndrome 4
familial encephalopathy with neuroserpin inclusion bodies
familial episodic pain syndrome 1
familial episodic pain syndrome 2
familial episodic pain syndrome 3
familial erythrocytosis 1
familial erythrocytosis 3
familial erythrocytosis 5
familial expansile osteolysis
familial hypocalciuric hypercalcemia +
familial male-limited precocious puberty
familial partial lipodystrophy type 2
familial partial lipodystrophy type 3
familial partial lipodystrophy type 4
familial progressive hyperpigmentation with or without hypopigmentation
familial temporal lobe epilepsy 1
familial temporal lobe epilepsy 2
familial temporal lobe epilepsy 3
familial temporal lobe epilepsy 4
familial temporal lobe epilepsy 5
familial temporal lobe epilepsy 6
familial temporal lobe epilepsy 7
familial temporal lobe epilepsy 8
Fanconi anemia complementation group R
Fanconi renotubular syndrome 1
Fanconi renotubular syndrome 3
Fanconi renotubular syndrome 4
Fanconi-like syndrome
Feingold syndrome
Feingold syndrome
Felty's syndrome
fetal akinesia deformation sequence syndrome +
fetal encasement syndrome
fetal valproate syndrome
FG syndrome
fibrochondrogenesis 2
fibrodysplasia ossificans progressiva
fibrogenesis imperfecta ossium
Finnish type amyloidosis
Floating-Harbor syndrome
Floating-Harbor syndrome
focal dermal hypoplasia
focal nonepidermolytic palmoplantar keratoderma 1
focal nonepidermolytic palmoplantar keratoderma 2
focal or diffuse nonepidermolytic palmoplantar keratoderma
focal segmental glomerulosclerosis 1
focal segmental glomerulosclerosis 2
focal segmental glomerulosclerosis 5
focal segmental glomerulosclerosis 7
focal segmental glomerulosclerosis 8
fragile X syndrome
Fraser syndrome +
Frasier syndrome
Frasier syndrome
frontometaphyseal dysplasia 2
Fuchs' heterochromic uveitis
Galloway-Mowat syndrome +
Gamstorp-Wohlfart syndrome
geleophysic dysplasia 2
geleophysic dysplasia 3
geroderma osteodysplasticum
giant axonal neuropathy 2
Gillespie syndrome
gnathodiaphyseal dysplasia
Goldberg-Shprintzen syndrome
Goldenhar syndrome
Gorham's disease
granular corneal dystrophy +
Greig cephalopolysyndactyly syndrome
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions
Guttmacher syndrome
Guttmacher syndrome
Hailey-Hailey disease
Hajdu-Cheney syndrome
Hallermann-Streiff syndrome
hand-foot-genital syndrome
hand-foot-genital syndrome
hawkinsinuria
Heinz body anemia
heparin cofactor II deficiency
hereditary alpha tryptasemia syndrome
hereditary arterial and articular multiple calcification syndrome
hereditary breast ovarian cancer syndrome
hereditary breast ovarian cancer syndrome
hereditary desmoid disease
hereditary diffuse gastric cancer
hereditary hemorrhagic telangiectasia
hereditary lymphedema IA
hereditary lymphedema IC
hereditary lymphedema ID
hereditary mixed polyposis syndrome 2
hereditary multiple exostoses
hereditary neuropathy with liability to pressure palsies
hereditary neutrophilia
hereditary sensory and autonomic neuropathy type 1A
hereditary sensory and autonomic neuropathy type 1C
hereditary sensory and autonomic neuropathy type 7
hereditary sensory neuropathy type 1B
hereditary sensory neuropathy type 1D
hereditary sensory neuropathy type 1E
hereditary sensory neuropathy type 1F
hereditary spastic paraplegia 10
hereditary spastic paraplegia 12
hereditary spastic paraplegia 13
hereditary spastic paraplegia 17
hereditary spastic paraplegia 19
hereditary spastic paraplegia 29
hereditary spastic paraplegia 31
hereditary spastic paraplegia 33
hereditary spastic paraplegia 36
hereditary spastic paraplegia 37
hereditary spastic paraplegia 38
hereditary spastic paraplegia 3A
hereditary spastic paraplegia 4
hereditary spastic paraplegia 41
hereditary spastic paraplegia 42
hereditary spastic paraplegia 6
hereditary spastic paraplegia 72
hereditary spastic paraplegia 73
hereditary spastic paraplegia 8
hereditary spherocytosis type 1
hereditary spherocytosis type 2
hereditary spherocytosis type 4
Hermansky-Pudlak syndrome +
high myopia-sensorineural deafness syndrome
histiocytosis-lymphadenopathy plus syndrome
holoprosencephaly +
holoprosencephaly 1
holoprosencephaly 11
holoprosencephaly 2
holoprosencephaly 3
holoprosencephaly 4
holoprosencephaly 5
holoprosencephaly 7
holoprosencephaly 9
Holt-Oram syndrome
Holt-Oram syndrome
Holzgreve-Wagner-Rehder Syndrome
hydrolethalus syndrome +
hyper IgE recurrent infection syndrome 1
hyperalphalipoproteinemia 1
hyperekplexia 1
hyperekplexia 3
hyperferritinemia-cataract syndrome
hyperferritinemia-cataract syndrome
hypertelorism, microtia, facial clefting syndrome
hypertension and brachydactyly syndrome
hypertension and brachydactyly syndrome
hypochondroplasia
hypogonadotropic hypogonadism 14 with or without anosmia
hypogonadotropic hypogonadism 15 with or without anosmia
hypogonadotropic hypogonadism 16 with or without anosmia
hypogonadotropic hypogonadism 17 with or without anosmia
hypogonadotropic hypogonadism 18 with or without anosmia
hypogonadotropic hypogonadism 19 with or without anosmia
hypogonadotropic hypogonadism 2 with or without anosmia
hypogonadotropic hypogonadism 20 with or without anosmia
hypogonadotropic hypogonadism 21 with or without anosmia
hypogonadotropic hypogonadism 3 with or without anosmia
hypogonadotropic hypogonadism 4 with or without anosmia
hypogonadotropic hypogonadism 5 with or without anosmia
hypogonadotropic hypogonadism 6 with or without anosmia
hypogonadotropic hypogonadism 9 with or without anosmia
hypomyelinating leukodystrophy 6
hypoparathyroidism-retardation-dysmorphism syndrome
hypophosphatasia +
hypophosphatemic nephrolithiasis/osteoporosis 1
hypophosphatemic nephrolithiasis/osteoporosis 2
hypoplastic or aplastic tibia with polydactyly
hypoplastic or aplastic tibia with polydactyly
hypotonia-cystinuria syndrome
hypotrichosis 1
hypotrichosis 11
hypotrichosis 12
hypotrichosis 13
hypotrichosis 2
hypotrichosis 3
hypotrichosis 4
hypotrichosis 5
hypotrichosis-lymphedema-telangiectasia syndrome
hypotrichosis-lymphedema-telangiectasia-renal defect syndrome
hypotrichosis-lymphedema-telangiectasia-renal defect syndrome
ichthyosis follicularis-alopecia-photophobia syndrome 1
ichthyosis vulgaris
IGSF1 deficiency syndrome
IMAGe syndrome
immunodeficiency 11B
immunodeficiency 13
immunodeficiency 14
immunodeficiency 15A
immunodeficiency 21
immunodeficiency 27B
immunodeficiency 31A
immunodeficiency 31C
immunodeficiency 32A
immunodeficiency 36
immunodeficiency 39
immunodeficiency 49
immunodeficiency 60
immunodeficiency 70
immunodeficiency-centromeric instability-facial anomalies syndrome +
inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1
inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2
inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3
inclusion body myopathy with Paget disease of bone and frontotemporal dementia +
infantile liver failure syndrome +
infantile or early childhood epileptic encephalopathy 1
infantile or early childhood epileptic encephalopathy 2
inflammatory bowel disease 21
inflammatory bowel disease 3
intellectual developmental disorder with short stature and behavioral abnormalities
intellectual disability-severe speech delay-mild dysmorphism syndrome
intrahepatic cholestasis of pregnancy 1
intrahepatic cholestasis of pregnancy 3
iridogoniodysgenesis syndrome
ischiocoxopodopatellar syndrome
isolated elevated serum creatine phosphokinase levels
isolated microphthalmia 7
ITM2B-related cerebral amyloid angiopathy 1
ITM2B-related cerebral amyloid angiopathy 2
IVIC syndrome
IVIC syndrome
Jackson-Weiss syndrome
Jalili syndrome
Jansen's metaphyseal chondrodysplasia
JMP syndrome
Johanson-Blizzard syndrome
juvenile glaucoma
juvenile polyposis syndrome
juvenile polyposis-hereditary hemorrhagic telangiectasia syndrome
juvenile polyposis-hereditary hemorrhagic telangiectasia syndrome
Kabuki syndrome
Kagami-Ogata syndrome
Kahrizi syndrome
KBG syndrome
Keipert syndrome
Kenny-Caffey syndrome +
Kenny-Caffey syndrome type 2
Kleefstra syndrome +
Kleefstra syndrome 1
Kleefstra syndrome 2
Klippel-Feil syndrome +
Klippel-Feil syndrome 1
Klippel-Feil syndrome 3
Klippel-Trenaunay syndrome
Kniest dysplasia
Kohlschutter-Tonz syndrome
Koolen de Vries syndrome
Koolen de Vries syndrome
LADD syndrome
LADD syndrome
Laron syndrome
Larsen syndrome
Larsen syndrome
Larsen-like syndrome B3GAT3 type
lateral meningocele syndrome
lateral meningocele syndrome
lattice corneal dystrophy
Laurence-Moon syndrome
Leber congenital amaurosis 11
Leber congenital amaurosis 13
Leber plus disease +
Lenz-Majewski hyperostotic dwarfism
Lenz-Majewski hyperostotic dwarfism
lethal congenital contracture syndrome +
Li-Fraumeni syndrome +
Li-Fraumeni syndrome +
linear nevus sebaceous syndrome
Loeys-Dietz syndrome +
Loeys-Dietz syndrome +
long QT syndrome 1
long QT syndrome 10
long QT syndrome 11
long QT syndrome 12
long QT syndrome 13
long QT syndrome 14
long QT syndrome 15
long QT syndrome 2
long QT syndrome 3
long QT syndrome 4
long QT syndrome 5
long QT syndrome 6
long QT syndrome 9
Lown-Ganong-Levine syndrome
lymphedema-distichiasis syndrome
lymphedema-distichiasis syndrome
Lynch syndrome +
Lynch syndrome +
macrocephaly-autism syndrome
macrocephaly-autism syndrome
Maffucci syndrome
malignant hyperthermia
mandibulofacial dysostosis with alopecia
mandibulofacial dysostosis, Guion-Almeida type
mandibulofacial dysostosis, Guion-Almeida type
Marinesco-Sjogren syndrome
Marshall-Smith syndrome
Martsolf syndrome
maturity-onset diabetes of the young +
McCune Albright syndrome
McKusick-Kaufman syndrome
MECP2 duplication syndrome
median arcuate ligament syndrome
MEDNIK syndrome
Meesmann corneal dystrophy 1
Meesmann corneal dystrophy 2
Meester-Loeys syndrome
mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations
megacystis-microcolon-intestinal hypoperistalsis syndrome
megalencephalic leukoencephalopathy with subcortical cysts 2B
Meier-Gorlin syndrome +
Meier-Gorlin syndrome 6
melanoma and neural system tumor syndrome
melanoma and neural system tumor syndrome
metachondromatosis
metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome
metatropic dysplasia
microcephaly and chorioretinopathy 1
microcephaly and chorioretinopathy 2
microcephaly and chorioretinopathy 3
microcephaly with or without chorioretinopathy, lymphedema, or mental retardation
microcephaly with or without chorioretinopathy, lymphedema, or mental retardation
microphthalmia with limb anomalies
midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis
Miller-Dieker lissencephaly syndrome
Miller-Dieker lissencephaly syndrome
mitochondrial DNA depletion syndrome 12a
Miura type epiphyseal chondrodysplasia
MLS syndrome +
monilethrix
mosaic variegated aneuploidy syndrome +
Mowat-Wilson syndrome
Mowat-Wilson syndrome
Muckle-Wells syndrome
Muckle-Wells syndrome
Muenke Syndrome
Mulchandani-Bhoj-Conlin syndrome
mulibrey nanism
Mullerian aplasia and hyperandrogenism
multicentric carpotarsal osteolysis syndrome
multicentric carpotarsal osteolysis syndrome
multicentric reticulohistiocytosis
multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia and hydranencephaly
multiple chemical sensitivity
multiple cutaneous and mucosal venous malformations
multiple endocrine neoplasia +
multiple endocrine neoplasia type 1
multiple endocrine neoplasia type 2A
multiple endocrine neoplasia type 2B
multiple endocrine neoplasia type 4
multiple epiphyseal dysplasia 1
multiple epiphyseal dysplasia 2
multiple epiphyseal dysplasia 3
multiple epiphyseal dysplasia 5
multiple epiphyseal dysplasia 6
multiple epiphyseal dysplasia with myopia and deafness
multiple epiphyseal dysplasia with myopia and deafness
multiple pterygium syndrome
myoclonic dystonia 11
myoclonic dystonia 15
myoclonic dystonia 26
myofibrillar myopathy 1
myofibrillar myopathy 2
myofibrillar myopathy 3
myofibrillar myopathy 4
myofibrillar myopathy 5
myofibrillar myopathy 6
N syndrome
Naegeli-Franceschetti-Jadassohn syndrome
nail-patella syndrome
nail-patella syndrome
Nance-Horan syndrome
Nasu-Hakola disease
nemaline myopathy 1
nemaline myopathy 4
nemaline myopathy 6
nephrotic syndrome type 4
neurodegeneration with brain iron accumulation 3
neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies
neurofibromatosis +
neurofibromatosis +
neurofibromatosis-Noonan syndrome
neurofibromatosis-Noonan syndrome
neurogenic scapuloperoneal syndrome Kaeser type
neurooculocardiogenitourinary syndrome
neurooculocardiogenitourinary syndrome
nevoid basal cell carcinoma syndrome
nevoid basal cell carcinoma syndrome
NFIA-related disorder
NFIA-related disorder
Nijmegen breakage syndrome
nonsyndromic congenital nail disorder 1
nonsyndromic congenital nail disorder 2
nonsyndromic congenital nail disorder 3
nonsyndromic congenital nail disorder 5
nonsyndromic congenital nail disorder 6
nonsyndromic congenital nail disorder 7
nonsyndromic congenital nail disorder 8
Noonan syndrome 1
Noonan syndrome 10
Noonan syndrome 3
Noonan syndrome 4
Noonan syndrome 5
Noonan syndrome 6
Noonan syndrome 7
Noonan syndrome 8
Noonan syndrome 9
Noonan syndrome with multiple lentigines +
Norrie disease
oblique facial clefting 1
ocular albinism with sensorineural deafness
oculoauricular syndrome
oculocerebrorenal syndrome
oculocutaneous albinism +
oculodentodigital dysplasia
Ogden syndrome
Ohdo syndrome +
Oliver-McFarlane syndrome
Ollier disease
Opitz-GBBB syndrome +
optic atrophy 1
optic atrophy 10
optic atrophy 3
optic atrophy 4
optic atrophy 5
optic atrophy 8
orofacial cleft +
orofacial cleft 1
orofacial cleft 13
orofacial cleft 6
orofaciodigital syndrome +
orofaciodigital syndrome X
osteogenesis imperfecta type 1
osteogenesis imperfecta type 2
osteogenesis imperfecta type 3
osteogenesis imperfecta type 4
osteogenesis imperfecta type 5
osteoglophonic dysplasia
osteoporosis-pseudoglioma syndrome
otospondylomegaepiphyseal dysplasia, autosomal dominant
ovarian dysgenesis 8
overhydrated hereditary stomatocytosis
pachyonychia congenita
pachyonychia congenita
Pallister-Hall syndrome
Pallister-Hall syndrome
palmoplantar keratoderma-deafness syndrome
palmoplantar keratoderma-deafness syndrome
palmoplantar keratoderma-esophageal carcinoma syndrome
palmoplantar keratoderma-esophageal carcinoma syndrome
pancreatic hypoplasia-diabetes-congenital heart disease syndrome
pancreatic hypoplasia-diabetes-congenital heart disease syndrome
PAPA syndrome
PAPA syndrome
paraganglioma
paramyotonia congenita of Von Eulenburg
parastremmatic dwarfism
Parkinson's disease 1
Parkinson's disease 17
Parkinson's disease 21
Parkinson's disease 22
Parkinson's disease 3
Parkinson's disease 4
Parkinson's disease 8
paroxysmal extreme pain disorder
paroxysmal nonkinesigenic dyskinesia 1
paroxysmal nonkinesigenic dyskinesia 2
PCWH syndrome
PCWH syndrome
Pelger-Huet anomaly
Pendred Syndrome
Perlman syndrome
permanent neonatal diabetes mellitus
Perrault syndrome +
Perry syndrome
Perry syndrome
persian gulf syndrome
Peters plus syndrome
Pfeiffer syndrome
PHARC syndrome
piebaldism
Pierson syndrome
pigmented paravenous chorioretinal atrophy
Pitt-Hopkins syndrome
Pitt-Hopkins syndrome
plasminogen deficiency type I
platelet-type bleeding disorder 12
platelet-type bleeding disorder 14
platelet-type bleeding disorder 15
platelet-type bleeding disorder 16
platelet-type bleeding disorder 17
platelet-type bleeding disorder 20
platelet-type bleeding disorder 3
platelet-type bleeding disorder 9
polycystic liver disease
popliteal pterygium syndrome
popliteal pterygium syndrome
post-cardiac arrest syndrome
postaxial acrofacial dysostosis
posterior amorphous corneal dystrophy
posterior polymorphous corneal dystrophy 1
posterior polymorphous corneal dystrophy 2
posterior polymorphous corneal dystrophy 4
Potocki-Shaffer syndrome
Prader-Willi syndrome
primary autosomal dominant microcephaly 18
primary ciliary dyskinesia 43
primary failure of tooth eruption
primary hypertrophic osteoarthropathy
progeria
progressive familial heart block type IA
progressive familial heart block type IB
progressive familial heart block type II
progressive myoclonus epilepsy 7
progressive osseous heteroplasia
progressive osseous heteroplasia
proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome
proprotein convertase 1/3 deficiency
protein C deficiency +
Proteus syndrome
prothrombin thrombophilia
proximal symphalangism
proximal symphalangism
prune belly syndrome
pseudo-TORCH syndrome 1
pseudoachondroplasia
PTEN hamartoma tumor syndrome
punctate palmoplantar keratoderma type II
punctate palmoplantar keratoderma type III
Qazi Markouizos syndrome
rapadilino syndrome
Rapp-Hodgkin syndrome
RASopathy +
renal coloboma syndrome
renal coloboma syndrome
retinal arterial tortuosity
retinal vasculopathy with cerebral leukodystrophy
retinitis pigmentosa 1
retinitis pigmentosa 10
retinitis pigmentosa 11
retinitis pigmentosa 13
retinitis pigmentosa 17
retinitis pigmentosa 18
retinitis pigmentosa 27
retinitis pigmentosa 33
retinitis pigmentosa 35
retinitis pigmentosa 37
retinitis pigmentosa 4
retinitis pigmentosa 42
retinitis pigmentosa 60
retinitis pigmentosa 63
retinitis pigmentosa 7
retinitis pigmentosa 70
retinitis pigmentosa 9
retinitis pigmentosa-deafness syndrome
Revesz syndrome
Reye syndrome
RIDDLE syndrome
ring dermoid of cornea
rippling muscle disease 2
Ritscher-Schinzel syndrome +
Roberts syndrome
Robinow syndrome +
Rubinstein-Taybi syndrome
Rubinstein-Taybi syndrome
Ruijs-Aalfs syndrome
SADDAN
SADDAN
Saethre-Chotzen syndrome
Saldino-Noonan syndrome
salt and pepper syndrome
SAPHO syndrome
SATB2-associated syndrome
Saul-Wilson syndrome
scalp-ear-nipple syndrome
scapuloperoneal spinal muscular atrophy
Schaaf-Yang syndrome
schizophrenia 1
schizophrenia 10
schizophrenia 11
schizophrenia 12
schizophrenia 15
schizophrenia 2
schizophrenia 3
schizophrenia 4
schizophrenia 5
schizophrenia 6
schizophrenia 7
schizophrenia 8
Schnyder corneal dystrophy
Schopf-Schulz-Passarge syndrome
Schwartz-Jampel syndrome 1
sclerosteosis 2
Seckel syndrome +
selective pituitary thyroid hormone resistance
Senior-Loken syndrome
Sensenbrenner syndrome
sepiapterin reductase deficiency
septooptic dysplasia
severe congenital neutropenia 1
SHORT syndrome
SHORT syndrome
Shukla-Vernon syndrome
Shwachman-Diamond syndrome
Simpson-Golabi-Behmel syndrome type 1
Simpson-Golabi-Behmel syndrome type 2
Sjogren-Larsson syndrome
snowflake vitreoretinal degeneration
solitary median maxillary central incisor
Sorsby's fundus dystrophy
Sotos syndrome
spastic ataxia 1
spastic ataxia 7
speech-language disorder-1
spermatogenic failure 10
spermatogenic failure 11
spermatogenic failure 12
spermatogenic failure 2
spermatogenic failure 3
spermatogenic failure 32
spermatogenic failure 36
spermatogenic failure 4
spermatogenic failure 8
spinal muscular atrophy with lower extremity predominance +
split hand-foot malformation 1
split hand-foot malformation 4
spondyloepimetaphyseal dysplasia, Missouri type
spondyloepimetaphyseal dysplasia, Strudwick type
spondyloepiphyseal dysplasia congenita
spondyloepiphyseal dysplasia Maroteaux type
spondylometaphyseal dysplasia Kozlowski type
steatocystoma multiplex
Stickler syndrome +
Stickler syndrome 1
Stickler syndrome 2
stiff skin syndrome
STING-associated vasculopathy with onset in infancy
Stormorken syndrome
subclavian steal syndrome
sudden infant death syndrome
Sweeney-Cox syndrome
Sweeney-Cox syndrome
syndactyly type 3
syndactyly type 4
syndactyly type 5
syndactyly-telecanthus-anogenital and renal malformations syndrome
syndactyly-telecanthus-anogenital and renal malformations syndrome
syndromic microphthalmia 3
syndromic microphthalmia 5
syndromic microphthalmia 6
TARP syndrome
tarsal-carpal coalition syndrome
Temple syndrome
temtamy preaxial brachydactyly syndrome
Temtamy syndrome
thiamine-responsive megaloblastic anemia syndrome
Thiel-Behnke corneal dystrophy
thrombocytopenia-absent radius syndrome
thrombophilia due to activated protein C resistance
thrombophilia due to HRG deficiency
thrombophilia due to thrombin defect
tibial muscular dystrophy
Tietz syndrome
Tietz syndrome
Tietze's syndrome
Timothy syndrome
Timothy syndrome
tooth and nail syndrome
torsion dystonia 1
torsion dystonia 13
torsion dystonia 4
torsion dystonia 6
torsion dystonia 7
torsion dystonia with onset in infancy
Townes-Brocks syndrome
Townes-Brocks syndrome
transthyretin amyloidosis
Treacher Collins syndrome
Treacher Collins syndrome
trichodontoosseous syndrome
trichodontoosseous syndrome
trichohepatoenteric syndrome +
trichorhinophalangeal syndrome type I
trichorhinophalangeal syndrome type I
trichorhinophalangeal syndrome type II
trichorhinophalangeal syndrome type II
trichorhinophalangeal syndrome type III
trichorhinophalangeal syndrome type III
trichothiodystrophy +
triple-A syndrome
tuberous sclerosis +
tuberous sclerosis +
tubular aggregate myopathy 1
tubular aggregate myopathy 2
type 1 diabetes mellitus 2
Ullrich congenital muscular dystrophy
ulnar-mammary syndrome
ulnar-mammary syndrome
urofacial syndrome
Usher syndrome +
uveal coloboma-cleft lip and palate-intellectual disability
uveal coloboma-cleft lip and palate-intellectual disability
VACTERL association +
Van den Ende-Gupta syndrome
Van der Woude syndrome
Van Maldergem syndrome +
vascular type Ehlers-Danlos syndrome
ventriculomegaly - cystic kidney disease
vertebral anomalies and variable endocrine and T-cell dysfunction
vertebral anomalies and variable endocrine and T-cell dysfunction
vertebral artery insufficiency
Vici syndrome
Vohwinkel syndrome
Vohwinkel syndrome
Waardenburg's syndrome +
Waardenburg's syndrome +
Waisman syndrome
Warburg micro syndrome +
Warsaw breakage syndrome
Weaver syndrome
Weaver syndrome
Weill-Marchesani syndrome
Werner syndrome
Weyers acrofacial dysostosis
WHIM syndrome
Williams-Beuren syndrome
Williams-Beuren syndrome
Winchester syndrome
Wiskott-Aldrich syndrome
Wissler-Fanconi syndrome
Wolcott-Rallison syndrome
Wolfram syndrome +
Worth syndrome
xeroderma pigmentosum +
XFE progeroid syndrome
yellow nail syndrome
Yunis-Varon syndrome
Zika virus congenital syndrome
Zollinger-Ellison syndrome
Child term(s)

is-a denotes an 'is-a' relationship