hypotrichosis 4
MONDO:0100522Mondo
Findings
No curated finding names hypotrichosis 4 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Congenital onset
HPO, annotations 2026-09-02
Features
6 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.
- Sparse eyebrowHPOHP:0045075
- 4 of 4 reported patients · Congenital onset
- Uncombable hairHPOHP:0030056
- 1 of 1 reported patient
- Sparse body hairHPOHP:0002231
- 3 of 4 reported patients
- AlopeciaHPOHP:0001596
- 1 of 4 reported patients
- Sparse scalp hairHPOHP:0002209
- 1 of 4 reported patients
- Sparse eyelashesHPOHP:0000653
Genes
2 genes
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.
- HRHGNC:5172
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2021
- HGNC:55085HGNC:55085
- Moderate · G2P · Autosomal dominant · 2025
Where it sits
- A kind of
Other names
5 names
Resolves to: hypotrichosis 4
- Also called
- hypotrichosis type 4hypotrichosis, Marie Unna type, 1HYPT4Marie Unna hereditary hypotrichosis 1MUHH1