Parent Terms |
Term With Siblings |
Child Terms |
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anterior segment dysgenesis +
Artificial Lens Implant Migration
autosomal genetic disease +
Camurati-Engelmann disease +
cardiofaciocutaneous syndrome +
cataract + A lens disease characterized by clouding of the lens inside the eye which leads to a decrease in vision. (DO)
catecholaminergic polymorphic ventricular tachycardia +
chondrodysplasia punctata +
Cornelia de Lange syndrome +
corticosteroid-binding globulin deficiency
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
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 +
gene duplication disease +
hereditary combined deficiency of vitamin K-dependent clotting factors +
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
Leber congenital amaurosis 10
Leber congenital amaurosis 3
Leber congenital amaurosis 7
multiple epiphyseal dysplasia due to collagen 9 anomaly +
osteogenesis imperfecta type 14
osteogenesis imperfecta type 6
posterior polymorphous corneal dystrophy 3
postural orthostatic tachycardia syndrome
primary congenital glaucoma +
Ritscher-Schinzel syndrome +
SHOX-related short stature
X-linked monogenic disease +
Y-linked monogenic disease +
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