wooly hair, autosomal recessive 3
Findings
No curated finding names wooly hair, autosomal recessive 3 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any wooly hair in which the cause of the disease is a mutation in the KRT25 gene.
Definition from the Mondo Disease Ontology (MONDO:0014765), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal recessive inheritance
HPO, annotations 2026-09-02
Features
5 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Curly hairHPOHP:0002212
- Sparse eyelashesHPOHP:0000653
- Sparse hairHPOHP:0008070
- Sparse scalp hairHPOHP:0002209
- Trichorrhexis nodosaHPOHP:0009886
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.
- KRT25HGNC:30839
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2020
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Moderate · G2P · Autosomal recessive · 2025
- Limited · PanelApp Australia · Autosomal dominant · 2025
Where it sits
Other names
7 names
Resolves to: wooly hair, autosomal recessive 3
- Also called
- ARWH3KRT25 woolly hair (disease)KRT25 wooly hair (disease)woolly hair (disease) caused by mutation in KRT25woolly hair, autosomal recessive type 3wooly hair (disease) caused by mutation in KRT25wooly hair, autosomal recessive type 3