Dataset | OMIM Gene-Disease Associations |
Category | disease or phenotype associations |
Type | phenotype |
Description | Focal facial dermal dysplasia type IV (FFDD4) is a rare focal facial dysplasia (FFDD; see this term), characterized by congenital isolated preauricular and/or cheek blister scar-like lesions. (Orphanet Rare Disease Ontology, Orphanet_398189) |
External Link | http://www.omim.org/entry/614974 |
Similar Terms | |
Downloads & Tools |
1 genes associated with the focal facial dermal dysplasia 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
Symbol | Name |
---|---|
CYP26C1 | cytochrome P450, family 26, subfamily C, polypeptide 1 |