Familial hyperprolactinemia

disorder

SNOMED 763715007CUI C4706551

Overview

Familial hyperprolactinemia 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.

Galactorrhea

Very frequent (80-99%)HP:0100829

Light or infrequent menstrual periods

Very frequent (80-99%)HP:0000876

Amenorrhea

Frequent (30-79%)HP:0000141

Hemorrhagic ovarian cyst

Frequent (30-79%)HP:0012886

Infertility

Frequent (30-79%)HP:0000789

Female hypogonadism

Occasional (5-29%)HP:0000134

Hypermenorrhea

Occasional (5-29%)HP:0000132

Osteopenia

Occasional (5-29%)HP:0000938

Osteoporosis

Occasional (5-29%)HP:0000939

Related Conditions

Autosomal dominant hereditary disorder(parent)

Familial disease(parent)

Hyperprolactinemia(parent)

Hereditary disorder of endocrine system(parent)

Hereditary disorder of nervous system(parent)

Quick Facts

SNOMED CT: 763715007
UMLS CUI: C4706551
Fully Specified Name: Familial hyperprolactinemia (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 9

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.