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Metadata
ID DOID:0061198
Name Bethlem myopathy 1A
Definition A Bethlem myopathy that has_material_basis_in heterozygous mutation in the COL6A1 gene on chromosome 21q22.
https://pubmed.ncbi.nlm.nih.gov/24038877/
Xrefs

MIM:158810

SKOS

exactMatch MIM:158810

broadMatch ORDO:610

broadMatch UMLS_CUI:C1834674

Parent Relationships

is_a autosomal dominant disease

is_a Bethlem myopathy

Subclass Logical Relationships

has material basis in some autosomal dominant inheritance

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