Dentinogenesis imperfecta - Shield's type III

disorder

SNOMED 234970006CUI C0399378

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.

Anterior open bite between upper and lower teeth

HP:0009102

Dentinogenesis imperfecta

HP:0000703

Periapical bone loss

HP:0000700

Pitting of tooth enamel

HP:0009722

Teeth with type iii dentinogenesis imperfecta

HP:0000694

Related Conditions

Dentinogenesis imperfecta(parent)

Quick Facts

SNOMED CT: 234970006
UMLS CUI: C0399378
Fully Specified Name: Dentinogenesis imperfecta - Shield's type III (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 5

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.