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DOID:0111239 - congenital muscular dystrophy-dystroglycanopathy type A10
Disease Ontology Definition:A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in RXYLT1 on 12q14.2.
Synonyms: MDDGA10, Walker-Warburg syndrome or muscle-eye-brain disease, TMEM5-related, congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A10,
Xenbase Genes :
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee