17 condition reports read genes linked to this trait

Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.

Show 13 more reports

Hyper-IgE SyndromeReads 1 of these genesSPINK5About this report
Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesTRPM4About this report
Epiphyseal and Spondyloepiphyseal DysplasiasReads 1 of these genesCOL2A1About this report
Hereditary Pheochromocytoma and ParagangliomaReads 1 of these genesSDHDAbout this report
Glycogen Storage DiseaseReads 1 of these genesLDHAAbout this report
Inherited Complement and Properdin DeficienciesReads 1 of these genesC1SAbout this report
Epidermolysis BullosaReads 1 of these genesCOL7A1About this report
Inherited IchthyosesReads 1 of these genesKRT10About this report
VitreoretinopathyReads 1 of these genesCOL2A1About this report
Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesIL36RNAbout this report
Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesTRPM4About this report
Other Inborn Errors of ImmunityReads 2 of these genesSPINK5C1SAbout this report
Congenital Disorders of GlycosylationReads 1 of these genesMPDU1About this report

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19 genes linked to Erythematous plaque

Changes in these genes cause rare conditions in which Erythematous plaque 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
AP1S3adaptor related protein complex 1 subunit sigma 3	Always	In 1 condition
IL36RNinterleukin 36 receptor antagonist	Always	In 1 condition
SPINK5serine peptidase inhibitor Kazal type 5	Always	In 1 condition
TRPM4transient receptor potential cation channel subfamily M member 4	Always	In 1 condition
C1Rcomplement C1r	Very often (80–99%)	In 1 condition
C1Scomplement C1s	Very often (80–99%)	In 1 condition
MEFVMEFV innate immunity regulator, pyrin	Very often (80–99%)	In 1 condition
PTPN6protein tyrosine phosphatase non-receptor type 6	Very often (80–99%)	In 1 condition
COL7A1collagen type VII alpha 1 chain	Often (30–79%)	In 1 condition
EBPEBP cholestenol delta-isomerase	Often (30–79%)	In 1 condition
GNA14G protein subunit alpha 14	Often (30–79%)	In 1 condition
HAVCR2hepatitis A virus cellular receptor 2	Often (30–79%)	In 1 condition
KRT10keratin 10	Often (30–79%)	In 1 condition
LDHAlactate dehydrogenase A	Often (30–79%)	In 1 condition
RASA1RAS p21 protein activator 1	Often (30–79%)	In 1 condition
SDHDsuccinate dehydrogenase complex subunit D	Often (30–79%)	In 1 condition
COL2A1collagen type II alpha 1 chain	Sometimes (5–29%)	In 1 condition
MPDU1mannose-P-dolichol utilization defect 1	Sometimes (5–29%)	In 1 condition
CARD14caspase recruitment domain family member 14	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.

Broader traits

Skin plaque

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.

Erythematous plaque

Summary

17 condition reports read genes linked to this trait

19 genes linked to Erythematous plaque

Broader traits

Where this comes from

Read the genes behind these traits in your own DNA.