Search Ontology:
Human Disease
congenital fibrosis of the extraocular muscles 5
- Term ID
- DOID:0081020
- Synonyms
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- Definition
- A congenital fibrosis of the extraocular muscles that has_material_basis_in homozygous or compound heterozygous mutation in the COL25A1 gene on chromosome 4q25. https://pubmed.ncbi.nlm.nih.gov/25500261/
- References
- Ontology
- Human Disease ( DOID:0081020 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models