Search Ontology:
Human Disease
muscular dystrophy-dystroglycanopathy type B15
- Term ID
- DOID:0112376
- Synonyms
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- 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 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models