Amelogenesis imperfecta, pigmented hypomaturation type

disorder

SNOMED 109474009CUI C1290537

Overview

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

Related Conditions

Amelogenesis imperfecta, hypomaturation type(parent)

Disorder of pigmentation(parent)

Recessive hereditary disorder (autosomal)(parent)

Oral lesion(parent)

Quick Facts

SNOMED CT: 109474009
UMLS CUI: C1290537
Fully Specified Name: Amelogenesis imperfecta, pigmented hypomaturation type (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.