RET Gene Mutation

Preferred Label : RET Gene Mutation;

NCIt synonyms : Ret Proto-Oncogene Mutation; Ret Proto-Oncogene Gene Mutation; RET/PTC Gene Mutation;

NCIt definition : A change in the structure of the RET gene.;

Détails

Origin ID

C43293;

UMLS CUI

C1711381;

Automatic exact mappings (from CISMeF team)
- RET gene mutation analysis [OBSOLETE LOINC component]
- RET gene mutations tested for [LOINC component]
Currated CISMeF NLP mapping
- RET gene mutation [MedDRA Preferred Term]
Molecular abnormality of diseases
- Sporadic Thyroid Gland Medullary Carcinoma [NCIt concept]
- Sporadic Thyroid Gland Micromedullary Carcinoma [NCIt concept]
- Thyroid Gland Mixed Medullary and Follicular Carcinoma [NCIt concept]
- Thyroid Gland Mixed Medullary and Follicular Cell-Derived Carcinoma [NCIt concept]
- Thyroid Gland Mixed Medullary and Papillary Carcinoma [NCIt concept]
Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
UMLS correspondences (same concept)
- RET gene mutation [MedDRA Preferred Term]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
- Pediatric Oncology Target Molecular Abnormalities Terminology [NCIt concept]
is_molecular_abnormality_of_disease
- Hereditary Thyroid Gland Medullary Carcinoma [NCIt concept]
- Multiple Endocrine Neoplasia Type 2 [NCIt concept]
- Multiple Endocrine Neoplasia Type 2A [NCIt concept]
- Multiple Endocrine Neoplasia Type 2B [NCIt concept]
- Neoplastic C-Cell Hyperplasia [NCIt concept]
- Recurrent Hereditary Thyroid Gland Medullary Carcinoma [NCIt concept]
- Unresectable Hereditary Thyroid Gland Medullary Carcinoma [NCIt concept]
molecular_abnormality_involves_gene
- RET Gene [NCIt concept]
- Receptor Tyrosine Kinase Gene [NCIt concept]

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