|
Feingold syndrome caused by mutation in MYCN
|
8115 |
|
|
autosomal dominant cerebellar ataxia type I caused by mutation in ATXN1
|
8119 |
|
|
autosomal recessive cerebellar ataxia-saccadic intrusion syndrome
|
11811 |
|
|
high altitude cerebral edema
|
21811 |
|
|
situs inversus, complex cardiac defects, and splenic defects, X-linked
|
C538116 |
|
|
night blindness, congenital stationary, type1i
|
32811 |
|
|
simple chronic conjunctivitis
|
4811 |
|
|
anomalous left coronary artery from the pulmonary artery
|
811 |
|
|
diabetes mellitus, deafness, nephropathy, and cerebral dysfunction photomyoclonus
|
C538113 |
|
|
complex cardiac defects, and splenic defects, X-linked situs inversus
|
C538116 |
|
