Disease #05050 (CFEOM3A (fibrosis of extraocular muscles, congenital, type 3A (CFEOM-3A)), OMIM:600638)
Official abbreviation |
CFEOM3A |
Name |
fibrosis of extraocular muscles, congenital, type 3A (CFEOM-3A) |
OMIM ID |
600638 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
TUBB3 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2015-09-23 11:00:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|