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
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