OBO ID: DOID:0112376
Term Name: muscular dystrophy-dystroglycanopathy type B15 Search Ontology:
Synonyms:
  • congenital muscular dystrophy DPM3-related
  • MDDGB15
Definition: A muscular dystrophy-dystroglycanopathy type B that has_material_basis_in homozygous or compound heterozygous mutation in DPM3 on chromosome 1q22. https://pubmed.ncbi.nlm.nih.gov/31469168/
References:
Ontology: Human Disease   (DOID:0112376)
OTHER muscular dystrophy-dystroglycanopathy type B15 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
DPM3 ?Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15 618992
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None