Autosomal recessive isolated somatotropin deficiency

disorder

SNOMED 18200000CUI C0271565

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Related Conditions

Pituitary dwarfism(parent)

Isolated somatotropin deficiency(parent)

Quick Facts

SNOMED CT: 18200000
UMLS CUI: C0271565
Fully Specified Name: Autosomal recessive isolated somatotropin 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.