Pontocerebellar Hypoplasia Type 7
| Disease Aliases (5) | Congenital pontocerebellar hypoplasia type 7 Non-syndromic pontocerebellar hypoplasia caused by mutation in toe1 Pch7 Pch7 - pontocerebellar hypoplasia type 7 Pontocerebellar hypoplasia-46,xy disorder of sex development syndrome |
Associated Genes (0) | |||||||
| Cross-references of Pontocerebellar hypoplasia type 7 | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |