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DO Term : congenital fibrosis of the extraocular muscles 5 [DOID:0081020] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A congenital fibrosis of the extraocular muscles that has_material_basis_in homozygous or compound heterozygous mutation in the COL25A1 gene on chromosome 4q25.

synonyms:
616219,
OMIM:616219

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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