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.
Lenz-Majewski hyperostosis syndrome
Always present (100%)
Senter syndrome
Frequent (30-79%)
Metaphyseal chondrodysplasia, McKusick type
Very frequent (80-99%)
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome
Very frequent (80-99%)
Hallermann-Streiff syndrome
Very frequent (80-99%)
Killian-Teschler-Nicola syndrome
Very frequent (80-99%)
Congenital ichthyosis of skin
Occasional (5-29%)
Borjeson-Forssman-Lehmann syndrome
Very frequent (80-99%)
Ectodermal dysplasia-ocular malformation syndrome
Frequent (30-79%)
Marshall syndrome
Frequent (30-79%)
Adams-Oliver syndrome
Very frequent (80-99%)
Oculodentodigital syndrome
Frequent (30-79%)
Ectrodactyly-ectodermal dysplasia-clefting syndrome
Occasional (5-29%)
Langer-Giedion syndrome
Occasional (5-29%)
Roberts-SC phocomelia syndrome
Very frequent (80-99%)
FG syndrome
Oral-facial-digital syndrome
Occasional (5-29%)
Hidrotic ectodermal dysplasia syndrome
Frequent (30-79%)
Hay-Wells syndrome of ectodermal dysplasia
Very frequent (80-99%)
Menkes kinky-hair syndrome
Very frequent (80-99%)
Cutis laxa-corneal clouding-oligophrenia syndrome
Very frequent (80-99%)
Weaver syndrome
Rothmund-Thomson syndrome
Frequent (30-79%)
Beaded hair
Very frequent (80-99%)
I-cell disease
Occasional (5-29%)
Related Symptoms
Quick Facts
- SNOMED CT
- 134006
- UMLS CUI
- C0232411
- Fully Specified Name
- Decreased 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.