Thyroid Gland Follicular Adenoma

Preferred Label : Thyroid Gland Follicular Adenoma;

NCIt synonyms : Adenoma of Thyroid; Thyroid Follicular Adenoma; Adenoma of Thyroid Gland; Thyroid Adenoma; Follicular Adenoma of the Thyroid; Adenoma of the Thyroid Gland;

NCIt related terms : ADENOMA, FOLLICULAR CELL, BENIGN; Follicular Adenoma of Thyroid; Follicular Adenoma of the Thyroid Gland; Thyroid Gland Adenoma; Follicular Adenoma of Thyroid Gland; Adenoma of the Thyroid;

NCIt definition : A benign, encapsulated neoplasm arising from the follicular cells of the thyroid gland. It may be associated with thyroid hormone secretion but it does not have malignant characteristics.;

Alternative definition : CDISC: A benign neoplasm arising from follicular cells of the thyroid gland.; NICHD: A non-malignant neoplasm of the thyroid gland arising from epithelial cells.;

Neoplastic status : Benign;

ICD-O code : 8330/0;

Details

Origin ID

C3502;

UMLS CUI

C0151468;

Automatic exact mappings (from CISMeF team)
- Follicular adenoma [ICD-O code]
- Follicular adenoma [ICD-11 Extension code]
- Follicular adenoma [ICD-9 code]
- Follicular adenoma of thyroid gland [ICD-11 More detail]
- Thyroid follicular adenoma [HPO term]
- adenoma [MeSH Descriptor]
- follicular adenoma [DO Concept]
- thyroid neoplasms [MeSH Descriptor]
Currated CISMeF NLP mapping
- Adenoma thyroid [MedDRA LLT]
- Follicular adenoma (morphologic abnormality) [SNOMED CT concept]
- THYROID ADENOMA [WHO-ART Preferred Term]
- Thyroid adenoma [HPO term]
- Thyroid adenoma [MedDRA Preferred Term]
- Thyroid adenoma NOS [MedDRA LLT]
- adenoma, follicular [MeSH concept]
- follicular adenoma [SNOMED Notion]
- thyroid adenoma [DO Concept]
- thyroid adenoma [Disease (Nov.)]
- thyroid adenoma [MeSH concept]
DO Cross reference
- thyroid adenoma [DO Concept]
Disease excludes abnormal cell
- Malignant Cell [NCIt concept]
- Malignant Endocrine Cell [NCIt concept]
- Malignant Epithelial Cell [NCIt concept]
- Neoplastic Smooth Muscle Cell [NCIt concept]
- Neoplastic Squamous Cell [NCIt concept]
Disease excludes normal cell origin
- Endocrine-Stromal Cell [NCIt concept]
Disease may have findings
- Radiation Toxicity [NCIt concept]
False automatic mappings
- Thyroid adenoma (disorder) [SNOMED CT concept]
- Thyroid adenoma (nontoxic) [MedDRA LLT]
- Thyroid follicular adenoma (disorder) [SNOMED CT concept]
Has associated anatomic sites
- Head and Neck [NCIt concept]
- Neck [NCIt concept]
- Thyroid Gland [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Adenoma thyroid [MedDRA LLT]
- THYROID ADENOMA [WHO-ART Preferred Term]
- Thyroid adenoma [MedDRA Preferred Term]
- Thyroid adenoma [HPO term]
- Thyroid adenoma (disorder) [SNOMED CT concept]
- Thyroid adenoma NOS [MedDRA LLT]
- Thyroid follicular adenoma [HPO term]
- Thyroid follicular adenoma (disorder) [SNOMED CT concept]
- thyroid adenoma [DO Concept]
- thyroid adenoma [Disease (Nov.)]
- thyroid adenoma [MeSH concept]
concept_is_in_subset
- CDISC SEND Terminology [NCIt concept]
- CDISC SEND Tumor Findings Results Terminology [NCIt concept]
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
- Clinical Data Interchange Standards Consortium Terminology [NCIt concept]
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]
- Mapped ICDO3.1 Morphology PT Terminology [NCIt concept]
- Mapped ICDO3.1 Morphology Terminology [NCIt concept]
- Mapped ICDO3.1 Terminology [NCIt concept]
- Mapped ICDO3.2 Morphology PT Terminology [NCIt concept]
- Mapped ICDO3.2 Morphology Terminology [NCIt concept]
- Mapped ICDO3.2 Terminology [NCIt concept]
- NCIt Neoplasm Core Terminology [NCIt concept]
- NICHD Terminology [NCIt concept]
- Pediatric Endocrinology Terminology [NCIt concept]
disease_excludes_cytogenetic_abnormality
- Loss of Chromosome 11q [NCIt concept]
- Loss of Chromosome 13q [NCIt concept]
- Loss of Chromosome 14q [NCIt concept]
- Loss of Chromosome 16q [NCIt concept]
- Loss of Chromosome 9p [NCIt concept]
- Loss of Chromosome 9q [NCIt concept]
disease_excludes_finding
- Borderline Lesion [NCIt concept]
- Capsular Invasion [NCIt concept]
- Ground Glass Nuclear Inclusion [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
- Mixed Neoplastic Glandular and Squamous Cell Population [NCIt concept]
- Nuclear Clearing [NCIt concept]
- Nuclear Grooves [NCIt concept]
- Nuclear Pseudoinclusion [NCIt concept]
- Tumor Vascular Invasion [NCIt concept]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Endocrine Cell [NCIt concept]
- Neoplastic Epithelial Cell [NCIt concept]
- Neoplastic Glandular Cell [NCIt concept]
- Neoplastic Thyroid Gland Follicular Cell [NCIt concept]
disease_has_finding
- Benign Cellular Infiltrate [NCIt concept]
- Encapsulated Mass [NCIt concept]
- Endocrine Differentiation [NCIt concept]
- Epithelial Component Present [NCIt concept]
- Follicular Structures Present [NCIt concept]
- Monoclonal Cellular Population Present [NCIt concept]
- Nodular Lesion [NCIt concept]
- Thyroglobulin-Positive Neoplastic Cells Present [NCIt concept]
disease_has_normal_cell_origin
- Epithelial Cell [NCIt concept]
- Thyroid Gland Follicular Cell [NCIt concept]
disease_has_normal_tissue_origin
- Epithelial Tissue [NCIt concept]
- Thyroid Gland Follicle [NCIt concept]
- Thyroid Gland Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Head and Neck [NCIt concept]
- Neck [NCIt concept]
- Thyroid Gland [NCIt concept]
disease_mapped_to_gene
- PAX8/PPARG Fusion Gene [NCIt concept]
disease_may_have_cytogenetic_abnormality
- Gain of Chromosome 12 [NCIt concept]
- Gain of Chromosome 5 [NCIt concept]
- Loss of Chromosome 10 [NCIt concept]
- Loss of Chromosome 13 [NCIt concept]
- Loss of Chromosome 19 [NCIt concept]
- Loss of Chromosome 3p [NCIt concept]
- Trisomy 7 [NCIt concept]
disease_may_have_molecular_abnormality
- HRAS Gene Mutation [NCIt concept]
- KRAS Gene Mutation [NCIt concept]
- NRAS Gene Mutation [NCIt concept]
may_be_associated_disease_of_disease
- Cowden Syndrome [NCIt concept]
pathogenesis_of_disease_involves_gene
- PAX8/PPARG Fusion Gene [NCIt concept]

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