Amelogenesis imperfecta - hypoplastic autosomal dominant - local

disorder

SNOMED 234961008CUI C0399368

Overview

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

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Amelogenesis imperfecta

HP:0000705

Related Conditions

Amelogenesis imperfecta, hypoplastic type(parent)

Autosomal dominant hereditary disorder(parent)

Quick Facts

SNOMED CT: 234961008
UMLS CUI: C0399368
Fully Specified Name: Amelogenesis imperfecta - hypoplastic autosomal dominant - local (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 1

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.