Panhypopituitarism - X-linked

disorder

SNOMED 237683004CUI C0342376

Overview

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

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Panhypopituitarism

HP:0000871

Pituitary dwarfism

HP:0000839

Related Conditions

Panhypopituitarism(parent)

X-linked hereditary disease(parent)

Hereditary disorder of endocrine system(parent)

Hereditary disorder of nervous system(parent)

Quick Facts

SNOMED CT: 237683004
UMLS CUI: C0342376
Fully Specified Name: X-linked panhypopituitarism (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 2

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.