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Ectodermal dysplasia with hair-tooth defects

disorder

SNOMED 239027006CUI C0406722

Overview

Ectodermal dysplasia with hair-tooth defects is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

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Hallermann-Streiff syndrome(child)

Uncombable hair, retinal pigmentary dystrophy, dental anomaly and brachydactyly syndrome(child)

Taurodontia with absent teeth and sparse hair syndrome(child)

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Ectodermal dysplasia with blindness syndrome(child)

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Kopysc Barczyk Krol syndrome(child)

Teebi Shaltout syndrome(child)

Ectodermal dysplasia syndactyly syndrome(child)

Ectodermal dysplasia with hair-tooth-nail defects(child)

Ectodermal syndrome with hair-tooth-sweating defects(child)

Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies(child)

Quick Facts

SNOMED CT: 239027006
UMLS CUI: C0406722
Fully Specified Name: Ectodermal dysplasia with hair-tooth defects (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.