Overview
Loss of hair is a finding that may indicate an underlying health condition requiring clinical evaluation.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Childhood type dermatomyositis
Frequent (30-79%)
Hallermann-Streiff syndrome
Very frequent (80-99%)
Biotinidase deficiency
Occasional (5-29%)
Killian-Teschler-Nicola syndrome
Frequent (30-79%)
Polyglandular autoimmune syndrome, type 1
Occasional (5-29%)
Congenital ichthyosis of skin
Frequent (30-79%)
Ehlers-Danlos syndrome, type 4
Occasional (5-29%)
Trichotillomania
Pili torti
Frequent (30-79%)
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome
Occasional (5-29%)
Tinea kerion
Frequent (30-79%)
Triglyceride storage disease with ichthyosis
Frequent (30-79%)
Alopecia totalis
Very frequent (80-99%)
Congenital erythropoietic porphyria
Poisoning by colchicine
Occasional (5-29%)
Mutilating keratoderma
Occasional (5-29%)
Autosomal recessive hypohidrotic ectodermal dysplasia syndrome
Frequent (30-79%)
African trypanosomiasis
Occasional (5-29%)
Leigh's disease
Very rare (1-4%)
Sarcoidosis
Occasional (5-29%)
Adams-Oliver syndrome
Occasional (5-29%)
Hereditary hemochromatosis
Hereditary acrodermatitis enteropathica
Very frequent (80-99%)
Lipid proteinosis
Frequent (30-79%)
Turner syndrome
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 278040002
- UMLS CUI
- C0002170
- Fully Specified Name
- Loss of hair (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.