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Human Disease

Ullrich congenital muscular dystrophy 1C

Term ID
DOID:0060943
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 or heterozygous mutation in the COL6A3 gene on chromosome 2q37. https://pubmed.ncbi.nlm.nih.gov/23622361/
References
Ontology
Human Disease   ( DOID:0060943 )
Relationships
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Genes Involved
Zebrafish Models