IGSF1 (immunoglobulin superfamily member 1) deficiency syndrome

disorder

SNOMED 771510006CUI C4749943

Overview

IGSF1 (immunoglobulin superfamily member 1) deficiency syndrome is a disorder.

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

Related Conditions

Reproductive system hereditary disorder(parent)

Central hypothyroidism(parent)

Hypertrophy of testis(parent)

Hereditary disorder of endocrine system(parent)

X-linked recessive hereditary disease(parent)

Quick Facts

SNOMED CT: 771510006
UMLS CUI: C4749943
Fully Specified Name: X-linked central congenital hypothyroidism with late-onset testicular enlargement (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.