hypotrichosis 9
MONDO:0013649Mondo
Findings
No curated finding names hypotrichosis 9 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 10q11.23-q22.3.
Definition from the Mondo Disease Ontology (MONDO:0013649), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal recessive inheritance
HPO, annotations 2026-09-02
Features
8 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
- 4 of 4 reported patients
- Sparse scalp hairHPOHP:0002209
- 4 of 4 reported patients
- Abnormal eyelash morphologyHPOHP:0000499
- 0 of 4 reported patients
- Abnormal nail morphologyHPOHP:0001597
- 0 of 4 reported patients
- Abnormality of the dentitionHPOHP:0000164
- 0 of 4 reported patients
- Hearing abnormalityHPOHP:0000364
- 0 of 4 reported patients
- HypohidrosisHPOHP:0000966
Where it sits
- A kind of
Other names
2 names
Resolves to: hypotrichosis 9
- Also called
- hypotrichosis type 9HYPT9