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Disease :

Primary Identifier  OMIM:613153 Name  MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5

Function

Disease --> HPO phenotype terms

Genomics

1 Genes

Disease

Disease --> HPO phenotype terms

 

Other

2 Alleles

3 Data Sets

3 Publications