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 the DPM3 gene on chromosome 1q22. https://pubmed.ncbi.nlm.nih.gov/31469168/
References:
Ontology: Human Disease   ( DOID:0112376 )
Relationships
is a type of:
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
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.