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 |
- |
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