Disease #05219 (CFM1;HFM (craniofacial microsomia (Goldenhar syndrome)), OMIM:164210)
| Official abbreviation |
CFM1;HFM |
| Name |
craniofacial microsomia (Goldenhar syndrome) |
| OMIM ID |
164210 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
16 |
| Phenotype entries for this disease |
16 |
| Associated with 1 gene |
SF3B2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2017-01-26 22:15:05 +01:00 (CET) |
| Date last edited |
2025-10-09 16:45:37 +02:00 (CEST) |
Individuals
|