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Congenital macroglossia

disorder
SNOMED 270516002CUI C0009677

Overview

Congenital macroglossia is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

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

Lingual hyperplasia
Very frequent (80-99%)HP:0000158
Abnormal hepatic glycogen storage
Very rare (1-4%)HP:0500030
Hypothyroidism
Very rare (1-4%)HP:0000821
Neurofibroma
Very rare (1-4%)HP:0001067

Quick Facts

SNOMED CT
270516002
UMLS CUI
C0009677
Fully Specified Name
Congenital macroglossia (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
4
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.