Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/615041
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Genes

1 genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
TMEM5 transmembrane protein 5