Overview
Congenital hypertrichosis is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Delayed eruption of teeth
Very frequent (80-99%)HP:0000684
Generalized hirsutism
Very frequent (80-99%)HP:0002230
Hypoacusis
Very frequent (80-99%)HP:0000365
Thick eyebrow
Very frequent (80-99%)HP:0000574
Tooth abnormalities
Very frequent (80-99%)HP:0000164
Abnormal skin colour
Frequent (30-79%)HP:0001000
Gingival hyperplasia
Occasional (5-29%)HP:0000212
Double eyebrow
HP:0010730
Hypertrichosis universalis
HP:0004540
Related Conditions
Hypertrichosis with congenital macrogingivae(child)
Congenital hypertrichosis lanuginosa(child)
Cervical hypertrichosis and peripheral neuropathy syndrome(child)
Amaurosis hypertrichosis syndrome(child)
Isolated anterior cervical hypertrichosis(child)
Congenital cataract with hypertrichosis and intellectual disability syndrome(child)
Wiedemann Steiner syndrome(child)
Hypertrichosis cubiti(child)
Barber-Say syndrome(child)
Congenital generalised hypertrichosis(child)
Congenital anomaly of hair(parent)
Hypertrichosis(parent)
Quick Facts
- SNOMED CT
- 56797000
- UMLS CUI
- C2936812
- Fully Specified Name
- Congenital hypertrichosis (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 9
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.