Familial multinodular goiter syndrome

disorder

SNOMED 1279836009CUI C5779622

Overview

Familial multinodular goiter syndrome 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.

Multinodular goiter

Always present (100%)HP:0005987

Basal cell nevus

Frequent (30-79%)HP:0002671

Colorectal polyps

Frequent (30-79%)HP:0200063

Ovarian neoplasm

Frequent (30-79%)HP:0100615

Pleuropulmonary blastoma

Frequent (30-79%)HP:0100528

Renal carcinoma

Frequent (30-79%)HP:0005584

Sertoli cell neoplasia

Frequent (30-79%)HP:0100619

Testicular seminoma

Frequent (30-79%)HP:0100617

Alveolar rhabdomyosarcoma

Very rare (1-4%)HP:0006779

Cerebellar medulloblastoma

Very rare (1-4%)HP:0007129

Medulloepithelioma

Very rare (1-4%)HP:0030071

Pilomatrixoma

Very rare (1-4%)HP:0030434

Thyroid carcinoma

Very rare (1-4%)HP:0002890

Related Conditions

Autosomal dominant hereditary disorder(parent)

Familial disease(parent)

Multinodular goitre(parent)

Hereditary disorder of endocrine system(parent)

Hereditary neoplastic syndrome(parent)

Quick Facts

SNOMED CT: 1279836009
UMLS CUI: C5779622
Fully Specified Name: Familial multinodular goiter syndrome (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.