Isolated corticotropin deficiency

disorder

SNOMED 80599001CUI C0271583

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.

ACTH deficiency

HP:0011748

Hypocortisolism

HP:0008163

Low blood sugar when fasting

HP:0003162

Seizures

HP:0001250

Slowed or blocked flow of bile from liver

HP:0001396

Small adrenal glands

HP:0000835

Yellowing of the skin

HP:0000952

Related Conditions

Congenital isolated adrenocorticotropic hormone deficiency(child)

Secondary hypoadrenalism(parent)

Quick Facts

SNOMED CT: 80599001
UMLS CUI: C0271583
Fully Specified Name: Isolated corticotropin deficiency (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 7

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.