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Hereditary opalescent dentine

disorder
SNOMED 234969005CUI C2973527

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.

Dentinogenesis imperfecta
HP:0000703
Yellow-brown discolored teeth
HP:0006286

Quick Facts

SNOMED CT
234969005
UMLS CUI
C2973527
Fully Specified Name
Dentinogenesis imperfecta - Shield's type II (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
2
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.