hypotrichosis 10
MONDO:0013650Mondo
Findings
No curated finding names hypotrichosis 10 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A hypotrichosis that has material basis in an autosomal recessive mutation on chromosome 7p22.3-p21.3.
Definition from the Mondo Disease Ontology (MONDO:0013650), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal recessive inheritance
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 body hairHPOHP:0002231
- 5 of 5 reported patients
- Sparse eyebrowHPOHP:0045075
- 5 of 5 reported patients
- Sparse eyelashesHPOHP:0000653
- 5 of 5 reported patients
- Sparse scalp hairHPOHP:0002209
- 5 of 5 reported patients
- Abnormal nail morphologyHPOHP:0001597
- 0 of 5 reported patients
- Abnormality of the dentitionHPOHP:0000164
- 0 of 5 reported patients
Where it sits
- A kind of
Other names
2 names
Resolves to: hypotrichosis 10
- Also called
- hypotrichosis type 10HYPT10