OntologiesCurators at RGD make annotations to genes, QTLs and strains using standardized vocabularies/ontologies. Your search returned annotations to the terms below.EFO: Experimental Factor Ontology
autosomal recessive limb-girdle muscular dystrophy type 2N
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2
muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B2
myopathy caused by variation in POMT2
GO: Molecular Function
dolichyl-phosphate-mannose-protein mannosyltransferase activity
RDO: RGD Disease Ontology
autosomal recessive limb-girdle muscular dystrophy type 2N
congenital muscular dystrophy-dystroglycanopathy type A2
muscular dystrophy-dystroglycanopathy type B2
Walker-Warburg syndrome
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