ZFIN Human Disease: congenital fibrosis of the extraocular muscles 5

OBO ID: DOID:0081020

Term Name:	congenital fibrosis of the extraocular muscles 5		Search Ontology:
Synonyms:
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:	OMIM:616219
Ontology:	Human Disease ( DOID:0081020 )

Relationships

is a type of:	autosomal recessive disease congenital fibrosis of the extraocular muscles autosomal recessive disease congenital fibrosis of the extraocular muscles Show first 5 Terms

OTHER congenital fibrosis of the extraocular muscles 5 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
COL25A1	col25a1	Fibrosis of extraocular muscles, congenital, 5	616219

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None