monogenic disease +
physical disorder +
glaucoma +

absolute glaucoma
agnathia-otocephaly complex
Alport syndrome +
angle-closure glaucoma +
anterior segment dysgenesis +
aqueous misdirection
arthrogryposis multiplex congenita +
autosomal dominant congenital deafness with onychodystrophy
autosomal genetic disease +
autosomal recessive congenital ichthyosis +
Bartter disease +
basal laminar drusen
bladder exstrophy-epispadias-cloacal exstrophy complex +
blepharophimosis
borderline glaucoma +
Brugada syndrome +
Camurati-Engelmann disease
cardiofaciocutaneous syndrome +
cataract +
catecholaminergic polymorphic ventricular tachycardia +
caudal regression syndrome
chondrodysplasia punctata +
ciliopathy +
cleft palate-lateral synechia syndrome
Compton-North congenital myopathy
cone-rod dystrophy +
congenital adrenal hyperplasia
congenital adrenal insufficiency
congenital afibrinogenemia
congenital amegakaryocytic thrombocytopenia
congenital aphakia
congenital bilateral absence of vas deferens +
congenital bile acid synthesis defect +
congenital central hypoventilation syndrome
congenital chylothorax
congenital contractural arachnodactyly
congenital diaphragmatic hernia
congenital diarrhea +
congenital disorder of glycosylation +
congenital epulis
congenital fibrosarcoma
congenital fibrosis of the extraocular muscles +
congenital generalized lipodystrophy +
congenital granular cell tumor
congenital heart block
congenital heart defects, hamartomas of tongue, and polysyndactyly
congenital heart disease +
congenital hemolytic anemia +
congenital hereditary endothelial dystrophy of cornea
congenital hypogammaglobulinemia
congenital hypoplastic anemia +
congenital hypothyroidism +
congenital hypotrichosis with juvenile macular dystrophy
congenital intrinsic factor deficiency
congenital lactase deficiency
congenital leptin deficiency
congenital megabladder
congenital mesoblastic nephroma +
congenital mirror movement disorder
congenital muscular dystrophy +
congenital myasthenic syndrome +
congenital myopathy 4A +
congenital nervous system abnormality +
congenital nystagmus +
congenital ptosis
congenital secretory chloride diarrhea 1
congenital secretory sodium diarrhea 3
congenital secretory sodium diarrhea 8
congenital stationary night blindness +
congenital stromal corneal dystrophy
congenital structural myopathy +
congenital sucrase-isomaltase deficiency
congenital syphilis +
congenital toxoplasmosis
congenital vertical talus
contractures, pterygia, and spondylocarpotarsal fusion syndrome +
Cornelia de Lange syndrome +
corticosteroid-binding globulin deficiency
cryptophthalmia +
developmental cardiac valvular defect
dilated cardiomyopathy 1BB
dilated cardiomyopathy 1EE
dilated cardiomyopathy 1FF
dilated cardiomyopathy 1G
dilated cardiomyopathy 1GG
dilated cardiomyopathy 1H
dilated cardiomyopathy 1I
dilated cardiomyopathy 1J
dilated cardiomyopathy 1K
dilated cardiomyopathy 1L
dilated cardiomyopathy 1M
dilated cardiomyopathy 1O
dilated cardiomyopathy 1P
dilated cardiomyopathy 1Q
dilated cardiomyopathy 1T
dilated cardiomyopathy 1W
dilated cardiomyopathy 1Z
epidermolysis bullosa with congenital localized absence of skin and deformity of nails
erythrokeratodermia variabilis +
familial hemophagocytic lymphohistiocytosis 5
familial nephrotic syndrome +
Fanconi anemia complementation group F
Fanconi anemia complementation group G
Fanconi anemia complementation group J
Fanconi anemia complementation group N
fetal akinesia deformation sequence syndrome +
gastroschisis
gene duplication disease +
hereditary combined deficiency of vitamin K-dependent clotting factors +
hypersecretion glaucoma
hypochondrogenesis
hypospadias
imperforate anus
infantile histiocytoid cardiomyopathy
inflammatory bowel disease 1
inflammatory bowel disease 10
inflammatory bowel disease 11
inflammatory bowel disease 12
inflammatory bowel disease 13
inflammatory bowel disease 14
inflammatory bowel disease 15
inflammatory bowel disease 16
inflammatory bowel disease 17
inflammatory bowel disease 18
inflammatory bowel disease 19
inflammatory bowel disease 2
inflammatory bowel disease 20
inflammatory bowel disease 22
inflammatory bowel disease 23
inflammatory bowel disease 24
inflammatory bowel disease 26
inflammatory bowel disease 27
inflammatory bowel disease 4
inflammatory bowel disease 5
inflammatory bowel disease 6
inflammatory bowel disease 7
inflammatory bowel disease 8
inflammatory bowel disease 9
isolated microphthalmia 4
Klippel-Feil syndrome +
lambda 5 deficiency
large congenital melanocytic nevus
laryngomalacia
Leber congenital amaurosis +
Leber congenital amaurosis 10
Leber congenital amaurosis 3
Leber congenital amaurosis 7
lethal congenital contracture syndrome +
lethal congenital glycogen storage disease of heart
linear skin defects with multiple congenital anomalies 1
linear skin defects with multiple congenital anomalies 2
linear skin defects with multiple congenital anomalies 3
Meckel's diverticulum
multiple congenital anomalies-hypotonia-seizures syndrome +
multiple epiphyseal dysplasia due to collagen 9 anomaly +
myotonia congenita +
neonatal diabetes mellitus with congenital hypothyroidism
neovascular glaucoma
neural tube defect +
non-congenital cyst of kidney
nonsyndromic congenital nail disorder +
Noonan syndrome +
omphalocele
open-angle glaucoma +
orofacial cleft +
osteogenesis imperfecta type 14
osteogenesis imperfecta type 6
palmoplantar keratoderma and congenital alopecia 1
palmoplantar keratoderma and congenital alopecia 2
pancreatic hypoplasia-diabetes-congenital heart disease syndrome
phacogenic glaucoma +
Poland syndrome
polydactyly
posterior polymorphous corneal dystrophy 3
postural orthostatic tachycardia syndrome
radioulnar synostosis
rapidly involuting congenital hemangioma
renal-hepatic-pancreatic dysplasia
Ritscher-Schinzel syndrome +
schizophrenia 13
schizophrenia 14
schizophrenia 16
schizophrenia 18
schizophrenia 9
severe congenital encephalopathy due to MECP2 mutation
severe congenital neutropenia +
SHOX-related short stature
Silver-Russell syndrome
spondyloepiphyseal dysplasia with congenital joint dislocations
steroid-induced glaucoma +
T-cell immunodeficiency, congenital alopecia, and nail dystrophy
TORCH syndrome
traumatic glaucoma
visceral heterotaxy +
X-linked monogenic disease +
Y-linked monogenic disease +
Zika virus congenital syndrome

hydrophthalmos +