distal myopathy 1
distal muscular dystrophy characterized by autosomal dominant inheritance that has material basis in mutation in the MYH7 gene on chromosome 14q11
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distal myopathy 1
Summary
distal myopathy 1 is a class of disease[1].
Key Facts
- distal myopathy 1's instance of is recorded as class of disease[2].
- distal myopathy 1's subclass of is recorded as distal muscular dystrophy[3].
- distal myopathy 1's subclass of is recorded as genetic disease[4].
- distal myopathy 1's subclass of is recorded as autosomal dominant disease[5].
- distal myopathy 1's OMIM ID is recorded as 160500[6].
- distal myopathy 1's KEGG ID is recorded as H01977[7].
- distal myopathy 1's Disease Ontology ID is recorded as DOID:0070197[8].
- distal myopathy 1's Orphanet ID is recorded as 59135[9].
- distal myopathy 1's genetic association is recorded as MYH7[10].
- distal myopathy 1's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0070197[11].
- distal myopathy 1's exact match is recorded as http://identifiers.org/doid/DOID:0070197[12].
- distal myopathy 1's GARD rare disease ID is recorded as 10769[13].
- distal myopathy 1's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- distal myopathy 1's UniProt disease ID is recorded as DI-01873[15].