Disease #04423 (CFEOM-5 (fibrosis of extraocular muscles, congenital, type 5 (CFEOM-5)), OMIM:616219)

Official abbreviation CFEOM-5
Name fibrosis of extraocular muscles, congenital, type 5 (CFEOM-5)
OMIM ID 616219
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene COL25A1
Associated tissues -
Disease features -
Remarks -