Familial erythrocytosis due to diphosphoglycerate mutase deficiency

disorder

SNOMED 127065001CUI C1264015

Overview

Familial erythrocytosis due to diphosphoglycerate mutase deficiency is a disorder.

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

Related Conditions

Hereditary pure erythrocytosis(parent)

Recessive hereditary disorder (autosomal)(parent)

Quick Facts

SNOMED CT: 127065001
UMLS CUI: C1264015
Fully Specified Name: Familial erythrocytosis due to diphosphoglycerate mutase deficiency (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.

Familial erythrocytosis due to diphosphoglycerate mutase deficiency — Symptoms, Testing & Specialists | Ltrl | Healos