Autosomal recessive severe congenital neutropenia due to JAGN1 (jagunal homolog 1) deficiency

disorder

SNOMED 783199003CUI C5190861

Overview

Autosomal recessive severe congenital neutropenia due to JAGN1 (jagunal homolog 1) 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: 783199003
UMLS CUI: C5190861
Fully Specified Name: Autosomal recessive severe congenital neutropenia due to jagunal homolog 1 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.