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Disease :

Primary Identifier  OMIM:615287 Name  MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13

Function

Disease --> HPO phenotype terms

Genomics

1 Genes

Disease

Disease --> HPO phenotype terms

 

Other

13 Alleles

3 Data Sets

1 Publications