Name
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 2
Synonmys
WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED
Classification
developmental,
eye,
genetic,
metabolism,
neurological
Associated Genes
POMT2
(Withdrawn symbols:
LGMD2N
)
Mouse Orthologs
Pomt2
(Withdrawn symbols:
A830009D15Rik,
AW046274
)
Source
OMIM:613150 (names, synonyms, disease associated genes),
Orphanet (disease classes),
HGNC, Ensembl, MGI (gene symbols, gene orthology)
HPO (phenotypes)
Orphanet (disease classes),
HGNC, Ensembl, MGI (gene symbols, gene orthology)
HPO (phenotypes)