Autosomal recessive severe congenital neutropenia due to C-X-C motif chemokine receptor 2 deficiency

disorder

SNOMED 783200000CUI C5190862

Overview

Autosomal recessive severe congenital neutropenia due to C-X-C motif chemokine receptor 2 deficiency is a disorder.

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

Related Conditions

Recessive hereditary disorder (autosomal)(parent)

Congenital neutropenia(parent)

Quick Facts

SNOMED CT: 783200000
UMLS CUI: C5190862
Fully Specified Name: Autosomal recessive severe congenital neutropenia due to C-X-C motif chemokine receptor 2 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.

Autosomal recessive severe congenital neutropenia due to C-X-C motif chemokine receptor 2 deficiency — Symptoms, Testing & Specialists | Ltrl