Familial papillary thyroid carcinoma with renal papillary neoplasia syndrome

disorder

SNOMED 716657000CUI C4274358

Overview

Familial papillary thyroid carcinoma with renal papillary neoplasia 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.

Abnormality of neck blood vessel

Very frequent (80-99%)HP:3000037

Head and neck cancer

Very frequent (80-99%)HP:0012288

Nodular goiter

Very frequent (80-99%)HP:0005994

Papillary carcinoma of thyroid

Very frequent (80-99%)HP:0002895

Papillary renal cell carcinoma

Very frequent (80-99%)HP:0006766

Abnormal lymph node histology

Frequent (30-79%)HP:0002733

Chronic noninfectious lymphadenopathy

Frequent (30-79%)HP:0002730

Thyroid goiter

Frequent (30-79%)HP:0000853

Breast carcinoma

Occasional (5-29%)HP:0003002

Chronic lung disease

Occasional (5-29%)HP:0006528

Colon cancer

Occasional (5-29%)HP:0003003

Frequent fractures

Occasional (5-29%)HP:0002757

Kidney cortical adenoma

Occasional (5-29%)HP:0006735

Renal oncocytoma

Occasional (5-29%)HP:0011798

Related Conditions

Familial neoplastic disease(parent)

Hereditary disorder of endocrine system(parent)

Hereditary neoplastic syndrome(parent)

Hereditary nephropathy(parent)

Papillary thyroid carcinoma with renal papillary neoplasia(parent)

Quick Facts

SNOMED CT: 716657000
UMLS CUI: C4274358
Fully Specified Name: Familial papillary thyroid carcinoma with renal papillary neoplasia syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 14

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.