Search Ontology:
Human Disease

Ullrich congenital muscular dystrophy 1B

Term ID
DOID:0060942
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 COL6A2 gene on chromosome 21q22. https://pubmed.ncbi.nlm.nih.gov/23622361/
References
Ontology
Human Disease   ( DOID:0060942 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models