Familial isolated pituitary adenoma

disorder

SNOMED 702375004CUI C2676191

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.

Prolactinoma

Always present (100%)HP:0006767

Acromegaly

Frequent (30-79%)HP:0033794

Pituitary adenoma

Frequent (30-79%)HP:0002893

Coarse face

HP:0000280

Disease of the heart muscle

HP:0001638

Elevated circulating growth hormone concentration

HP:0000845

Galactorrhea

HP:0100829

High blood pressure

HP:0000822

Increased circulating insulin-like growth factor 1 concentration

HP:0030269

Left ventricular wall hypertrophy

HP:0001712

Menstrual irregularity

HP:0000858

Pituitary somatotropinoma

HP:0011760

Prolactin excess

HP:0000870

Related Conditions

Autosomal dominant hereditary disorder(parent)

Hereditary disorder of endocrine system(parent)

Hereditary disorder of nervous system(parent)

Pituitary adenoma(parent)

Quick Facts

SNOMED CT: 702375004
UMLS CUI: C2676191
Fully Specified Name: Familial isolated pituitary adenoma (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 13

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.