Trait
Seborrheic dermatitis
Seborrheic dermatitis is a form of eczema which is closely related to dandruff. It causes dry or greasy peeling of the scalp, eyebrows, and face, and sometimes trunk.
Summary
- Also called
- Seborrhea, Seborrheic eczema
Reference genomeGRCh38hg38
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Get my Genome Test28 genes linked to Seborrheic dermatitis
Changes in these genes cause rare conditions in which Seborrheic dermatitis is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| SLCO2A1solute carrier organic anion transporter family member 2A1 | Always | In 3 conditions |
| SPINK5serine peptidase inhibitor Kazal type 5 | Always | In 1 condition |
| TRAF3IP2TRAF3 interacting protein 2 | Always | In 1 condition |
| AIPAHR interacting HSP90 co-chaperone | Very often (80–99%) | In 1 condition |
| CIB1calcium and integrin binding 1 | Very often (80–99%) | In 1 condition |
| GPR101G protein-coupled receptor 101 | Very often (80–99%) | In 1 condition |
| HPGD15-hydroxyprostaglandin dehydrogenase | Very often (80–99%) | In 2 conditions |
| IL7interleukin 7 | Very often (80–99%) | In 1 condition |
| TMC6transmembrane channel like 6 | Very often (80–99%) | In 1 condition |
| TMC8transmembrane channel like 8 | Very often (80–99%) | In 1 condition |
| ARVCFARVCF delta catenin family member | Often (30–79%) | In 1 condition |
| COMTcatechol-O-methyltransferase | Often (30–79%) | In 1 condition |
| GP1BBglycoprotein Ib platelet subunit beta | Often (30–79%) | In 1 condition |
| HIRAhistone cell cycle regulator | Often (30–79%) | In 1 condition |
| JMJD1Cjumonji domain containing 1C | Often (30–79%) | In 1 condition |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Often (30–79%) | In 2 conditions |
| RREB1ras responsive element binding protein 1 | Often (30–79%) | In 1 condition |
| SEC24CSEC24 homolog C, COPII component | Often (30–79%) | In 1 condition |
| TBX1T-box transcription factor 1 | Often (30–79%) | In 2 conditions |
| UFD1ubiquitin recognition factor in ER associated degradation 1 | Often (30–79%) | In 1 condition |
| CARMIL2capping protein regulator and myosin 1 linker 2 | Sometimes (5–29%) | In 1 condition |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Sometimes (5–29%) | In 1 condition |
| SLC39A7solute carrier family 39 member 7 | Sometimes (5–29%) | In 1 condition |
| TKTtransketolase | Sometimes (5–29%) | In 1 condition |
| BTDbiotinidase | Not recorded | In 1 condition |
| MCCC2methylcrotonyl-CoA carboxylase subunit 2 | Not recorded | In 1 condition |
| RBM8ARNA binding motif protein 8A | Not recorded | In 1 condition |
| ZNF750zinc finger protein 750 | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
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Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
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