seborrheic dermatitis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A dermatitis that is an inflammatory skin condition resulting in flaky, white to yellowish scales on oily areas such as the scalp or inside the ear, which is caused due to a combination of an over production of skin oil and irritation from a yeast Malassezia furfur. The symptoms include itching, skin lesions and scales, redness, plaques and hair loss. (Human Disease Ontology, DOID_8741)
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16 genes associated with the seborrheic dermatitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ARVCF armadillo repeat gene deleted in velocardiofacial syndrome
BTD biotinidase
C5 complement component 5
COMT catechol-O-methyltransferase
GP1BB glycoprotein Ib (platelet), beta polypeptide
HIRA histone cell cycle regulator
HPGD hydroxyprostaglandin dehydrogenase 15-(NAD)
MCCC2 methylcrotonoyl-CoA carboxylase 2 (beta)
PIGA phosphatidylinositol glycan anchor biosynthesis, class A
RBM8A RNA binding motif protein 8A
SLCO2A1 solute carrier organic anion transporter family, member 2A1
TBX1 T-box 1
TMC6 transmembrane channel-like 6
TMC8 transmembrane channel-like 8
UFD1L ubiquitin fusion degradation 1 like (yeast)
ZNF750 zinc finger protein 750