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Reference

Evidence

Compounds
Outcomes
Proteins
Interactions
Papers
Articles

Chemistry

Reactions
Reach

Reference layer

Pathways
Processes
Anatomy
Cell types
Organisms
Materials
Assessments
Diseases

Atlas Graph Twin Access

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A reference for what the literature reports. Not medical advice.

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ectodermal dysplasia WNT10A related

MONDO:0100358Mondo

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Findings

No curated finding names ectodermal dysplasia WNT10A related yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Genes

1 gene

Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.

WNT10AHGNC:13829
- Definitive · ClinGen · Semidominant · 2022
- Definitive · Illumina · Semidominant · 2021
- Definitive · Natera · Semidominant · 2023
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Strong · PanelApp Australia · Autosomal dominant · 2025

Where it sits

A kind of: ectodermal dysplasia syndrome
Narrower terms (3): odonto-onycho-dermal dysplasia
Schöpf-Schulz-Passarge syndrome
tooth agenesis, selective, 4