FNMTC - familial nonmedullary thyroid carcinoma

disorder

SNOMED 786038001CUI C5191836

Overview

FNMTC - familial nonmedullary thyroid carcinoma 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

Follicular thyroid carcinoma

Very frequent (80-99%)HP:0006731

Head and neck tumour

Very frequent (80-99%)HP:0012288

Nodular goiter

Very frequent (80-99%)HP:0005994

Abnormal lymph node histology

Frequent (30-79%)HP:0002733

Chronic noninfectious lymphadenopathy

Frequent (30-79%)HP:0002730

Thyroid goiter

Frequent (30-79%)HP:0000853

Bone pain

Occasional (5-29%)HP:0002653

Chronic lung disease

Occasional (5-29%)HP:0006528

Colon cancer

Occasional (5-29%)HP:0003003

Pain

Occasional (5-29%)HP:0012531

Papillary carcinoma of thyroid

Occasional (5-29%)HP:0002895

Papillary renal cell carcinoma

Occasional (5-29%)HP:0006766

Spinal cord compression

Occasional (5-29%)HP:0002176

Varying degree of multiple fractures

Occasional (5-29%)HP:0002757

Related Conditions

Primary malignant neoplasm of thyroid gland(parent)

Familial neoplastic disease(parent)

Carcinoma of thyroid(parent)

Hereditary disorder of endocrine system(parent)

Primary malignant epithelial neoplasm of endocrine gland(parent)

Quick Facts

SNOMED CT: 786038001
UMLS CUI: C5191836
Fully Specified Name: Familial nonmedullary primary thyroid carcinoma (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 15

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.