focal facial dermal dysplasia 4 Gene Set

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
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Genes

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