Mahvash disease

disorder

SNOMED 1228875006CUI C4763635

Overview

Mahvash disease is a disorder.

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

Signs & Symptoms

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

Increased glucagon level

Always present (100%)HP:0030688

Palpitations

Always present (100%)HP:0001962

Pancreatic alpha-cell hyperplasia

Always present (100%)HP:4000061

Vertigo

Always present (100%)HP:0002321

Anomaly of the biliary tract

Frequent (30-79%)HP:0012440

Gallstones

Frequent (30-79%)HP:0001081

Gastro pain

Frequent (30-79%)HP:0002027

Glucagonoma

Frequent (30-79%)HP:0030404

increased risk of pancreatic cancer

Frequent (30-79%)HP:0002894

NIDDM

Frequent (30-79%)HP:0005978

Recurring pancreatitis

Frequent (30-79%)HP:0100027

Related Conditions

Developmental hereditary disorder(parent)

Digestive system hereditary disorder(parent)

Hereditary disorder of endocrine system(parent)

Recessive hereditary disorder (autosomal)(parent)

Hyperplasia of islet alpha cells with glucagon excess(parent)

Quick Facts

SNOMED CT: 1228875006
UMLS CUI: C4763635
Fully Specified Name: Glucagon receptor-related hyperglucagonemia (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 11

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.