|
adult polyglucosan body disease
|
9897 |
|
|
neuronal, 7 ceroid lipofuscinosis
|
C563989 |
|
|
mental retardation, callosal agenesis, heminasal hypoplasia, microphthalmia, and atypical clefting short stature
|
C566989 |
|
|
charcot-marie-tooth disease, autosomal dominant, type 2b
|
C537989 |
|
|
familial polycythemia caused by mutation in VHL
|
9892 |
|
|
Toxoplasma gondii caused disease or disorder
|
5989 |
|
|
Mumps virus caused disease or disorder
|
989 |
|
|
charcot-marie-tooth disease, axonal, type 2b
|
C537989 |
|
|
type 2b charcot-marie-tooth disease
|
C537989 |
|
|
type 2b charcot-marie-tooth neuropathy
|
C537989 |
|
|
9q subtelomeric deletion syndrome
|
19896 |
|
|
citrulline transport defect
|
8989 |
|
|
Lactogen receptor defect of chorion
|
9899 |
|
|
alpha 1-antitrypsin deficiencies
|
D019896 |
|
