|
autosomal recessive 1b deafness
|
C567213 |
|
|
autosomal dominant 4 mental retardation
|
C567240 |
|
|
1.35-mb chromosome 1q21.1 deletion syndrome
|
C567291 |
|
|
autosomal dominant 2b deafness
|
C567214 |
|
|
diamond-blackfan anemia 5
|
C567280 |
|
|
autosomal dominant 5 mental retardation
|
C567234 |
|
|
infantile hypertrophic, 5 pyloric stenosis
|
C567283 |
|
|
autosomal dominant 59 deafness
|
C567216 |
|
|
diamond-blackfan anemia 7
|
C567254 |
|
|
infection by Blastomyces dermatitidis
|
5672 |
|
|
retinitis pigmentosa 7 with bull's-eye maculopathy
|
C567264 |
|
|
diamond-blackfan anemia 8
|
C567253 |
|
|
autosomal dominant 3 mental retardation
|
C567241 |
|
|
hearing loss, ataxia, retinitis pigmentosa, and cataract polyneuropathy
|
C567203 |
|
