OBO ID: DOID:0110638
Term Name: congenital muscular dystrophy merosin-positive Search Ontology:
Synonyms:
Definition: A congenital muscular dystrophy characterized by autosomal recessive inheritance of generalized muscle weakness and hypotonia without arthrogryposis or central nervous system involvement that has_material_basis_in mutation in the chromosome region 4p16.3. (2)
References:
Ontology: Human Disease   (DOID:0110638)
OTHER congenital muscular dystrophy merosin-positive PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None