Overview
Congenital alopecia is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Congenital localised alopecia(child)
Congenital alopecia with keratin cysts(child)
Congenital generalised alopecia(child)
Vertical alopecia(child)
Sutural alopecia(child)
Triangular alopecia(child)
Atrichia congenita(child)
Autosomal recessive palmoplantar keratoderma and congenital alopecia syndrome(child)
Autosomal dominant palmoplantar keratoderma and congenital alopecia(child)
Choroidal atrophy and alopecia syndrome(child)
Shokeir syndrome(child)
Severe T-cell immunodeficiency, congenital alopecia, nail dystrophy syndrome(child)
Intellectual disability, balding, patella luxation, acromicria syndrome(child)
Gomez Lopez Hernandez syndrome(child)
Ichthyosis, alopecia, eclabion, ectropion, intellectual disability syndrome(child)
Odonto onycho dysplasia with alopecia syndrome(child)
Thumb deformity, alopecia, pigmentation anomaly syndrome(child)
ANE syndrome(child)
PARC syndrome(child)
Ectodermal dysplasia syndactyly syndrome(child)
Quick Facts
- SNOMED CT
- 2965006
- UMLS CUI
- C0265992
- Fully Specified Name
- Congenital alopecia (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
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.