autosomal recessive limb-girdle muscular dystrophy type 2W
autosomal recessive limb-girdle muscular dystrophy that has material basis in compound heterozygous mutation in the LIMS2 gene on chromosome 2q14
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autosomal recessive limb-girdle muscular dystrophy type 2W
Summary
autosomal recessive limb-girdle muscular dystrophy type 2W is a rare disease[1].
Key Facts
- autosomal recessive limb-girdle muscular dystrophy type 2W's instance of is recorded as rare disease[2].
- autosomal recessive limb-girdle muscular dystrophy type 2W's instance of is recorded as class of disease[3].
- autosomal recessive limb-girdle muscular dystrophy type 2W's subclass of is recorded as autosomal recessive limb-girdle muscular dystrophy[4].
- autosomal recessive limb-girdle muscular dystrophy type 2W's subclass of is recorded as neuromuscular disease with dilated cardiomyopathy[5].
- autosomal recessive limb-girdle muscular dystrophy type 2W's OMIM ID is recorded as 616827[6].
- autosomal recessive limb-girdle muscular dystrophy type 2W's Disease Ontology ID is recorded as DOID:0110288[7].
- autosomal recessive limb-girdle muscular dystrophy type 2W's Orphanet ID is recorded as 466801[8].
- autosomal recessive limb-girdle muscular dystrophy type 2W's genetic association is recorded as LIMS2[9].
- autosomal recessive limb-girdle muscular dystrophy type 2W's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110288[10].
- autosomal recessive limb-girdle muscular dystrophy type 2W's exact match is recorded as http://identifiers.org/doid/DOID:0110288[11].
- autosomal recessive limb-girdle muscular dystrophy type 2W's UMLS CUI is recorded as C4225192[12].
- autosomal recessive limb-girdle muscular dystrophy type 2W's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- autosomal recessive limb-girdle muscular dystrophy type 2W's Mondo ID is recorded as MONDO_0014788[14].