Term Name: | Ullrich congenital muscular dystrophy 1A |
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Synonyms: | |
Definition: | An Ullrich congenital muscular dystrophy characterized by generalized muscle weakness and striking hypermobility of distal joints in conjunction with variable contractures of more proximal joints and normal intelligence that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the COL6A1 gene on chromosome 21q22. |
Ontology: | Human Disease [DOID:0060946] ( DOID:0060946 ) |