|
short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies
|
60649.0 |
|
|
extracranial neuroblastoma
|
2749.0 |
|
|
acute motor axonal neuropathy
|
20349.0 |
|
|
benign neoplasm of stomach
|
21449.0 |
|
|
congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay
|
60549.0 |
|
|
hereditary optic neuropathy
|
20249.0 |
|
|
autosomal recessive nonsyndromic deafness 84A
|
13249.0 |
|
|
pontocerebellar hypoplasia type 10
|
14349.0 |
|
|
Charcot-Marie-Tooth disease type 2B
|
10949.0 |
|
|
attention deficit-hyperactivity disorder, susceptibility to, 1
|
12149.0 |
|
|
conjunctival degeneration
|
949.0 |
|
