|
autosomal recessive nonsyndromic deafness 105
|
14849.0 |
|
|
microcephaly 8, primary, autosomal recessive
|
13849.0 |
|
|
neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies
|
32849.0 |
|
|
inflammatory bowel disease 29
|
54849.0 |
|
|
congenital stenosis of cervical medullary canal
|
22849.0 |
|
|
Siegler-Brewer-Carey syndrome
|
17849.0 |
|
|
longitudinal vaginal septum
|
15849.0 |
|
|
obsolete Nakajo-Nishimura syndrome
|
16849.0 |
|
|
fibrogenesis imperfecta ossium
|
849.0 |
|
|
chronic orbital inflammation
|
1849.0 |
|
