C1859093 |
Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism |
DO |
Boucher-Neuhauser syndrome
|
0111265 |
C1859093 |
Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism |
MONDO |
ataxia-hypogonadism-choroidal dystrophy syndrome
|
0008980 |
C1859093 |
Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism |
MSH |
Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism
|
C565850 |
C1859093 |
Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism |
OMIM |
BOUCHER-NEUHAUSER SYNDROME
|
215470 |
C1859093 |
Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism |
OMIM |
SPINOCEREBELLAR ATAXIA, HYPOGONADOTROPIC HYPOGONADISM, AND CHORIORETINAL DYSTROPHY
|
215470 |
C1859093 |
Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism |
ORDO |
Ataxia-hypogonadism-choroidal dystrophy syndrome
|
1180 |