Amelogenesis imperfecta - hypoplastic autosomal dominant - rough

disorder

SNOMED 234963006CUI C0399370

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Related Conditions

Amelogenesis imperfecta, hypoplastic type(parent)

Autosomal dominant hereditary disorder(parent)

Quick Facts

SNOMED CT: 234963006
UMLS CUI: C0399370
Fully Specified Name: Amelogenesis imperfecta - hypoplastic autosomal dominant - rough (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.