Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Bloom syndrome
Coffin-Siris syndrome
Very frequent (80-99%)
Insulin receptor defect
Always present (100%)
Schinzel-Giedion syndrome
Congenital erythropoietic porphyria
Leigh's disease
Frequent (30-79%)
Pineal hyperplasia AND diabetes mellitus syndrome
Frequent (30-79%)
Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes
Occasional (5-29%)
Papillon-Lefèvre syndrome
Occasional (5-29%)
Variegate porphyria
Occasional (5-29%)
Porphyria cutanea tarda
Occasional (5-29%)
Mannosidosis
Mucopolysaccharidosis, MPS-II
Marshall-Smith syndrome
Very frequent (80-99%)
Acromegaly
Occasional (5-29%)
Mucopolysaccharidosis, MPS-III-C
Occasional (5-29%)
POEMS syndrome
Frequent (30-79%)
Kasabach-Merritt syndrome
Very rare (1-4%)
Acquired generalized lipodystrophy
Frequent (30-79%)
Leprechaunism syndrome
Very frequent (80-99%)
Deficiency of alpha-mannosidase
Congenital porphyria
GM1 gangliosidosis
Infantile gangliosidosis with bony involvement
Tufted angioma of skin
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 271607001
- UMLS CUI
- C0020555
- Fully Specified Name
- Excessive hair growth (finding)
- Associated Conditions
- 25
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.