Disease: Spastic Ataxia 7, Autosomal Dominant

Name
Spastic Ataxia 7, Autosomal Dominant
Synonmys
MIOSIS, CONGENITAL, WITH SPASTIC ATAXIA , SPASTIC ATAXIA WITH CONGENITAL MIOSIS
Classification
eye, genetic, neurological
Associated Genes
-
Mouse Orthologs
-
Source
OMIM:108650 (names, synonyms, disease associated genes),
Orphanet (disease classes),
HGNC, Ensembl, MGI (gene symbols, gene orthology)
HPO (phenotypes)

Mouse Models

Learn about how to interpret our results in the Disease Models Help pages

No mouse models associated with OMIM:108650 by orthology to a human gene.

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