Autosomal recessive agammaglobulinaemia due to FNIP1 deficiency

disorder

SNOMED 1351648007CUI C5968862

Overview

Autosomal recessive agammaglobulinaemia due to FNIP1 deficiency is a disorder.

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

Related Conditions

Congenital agammaglobulinemia(parent)

Recessive hereditary disorder (autosomal)(parent)

Cardiovascular system hereditary disorder(parent)

Hereditary disorder of immune system(parent)

Heart disease(parent)

Quick Facts

SNOMED CT: 1351648007
UMLS CUI: C5968862
Fully Specified Name: Autosomal recessive agammaglobulinemia due to folliculin interacting protein 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.