STK11 Gene Mutation

Preferred Label : STK11 Gene Mutation;

NCIt synonyms : Serine/Threonine Kinase 11 Gene Mutation; STK11 Mutation; LKB1 Gene Mutation; Liver Kinase B1 Gene Mutation;

NCIt definition : A change in the nucleotide sequence of the STK11 gene.;

NCI Metathesaurus CUI : CL512235;

Détails

Origin ID

C128825;

UMLS CUI

C4287907;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
is_molecular_abnormality_of_disease
- Colorectal Peutz-Jeghers Polyp [NCIt concept]
- Intratubular Large Cell Hyalinizing Sertoli Cell Neoplasia [NCIt concept]
- Peutz-Jeghers Polyp [NCIt concept]
- Peutz-Jeghers Polyp of the Small Intestine [NCIt concept]
- Peutz-Jeghers Polyp of the Stomach [NCIt concept]
- Peutz-Jeghers Syndrome [NCIt concept]
is_not_molecular_abnormality_of_disease
- Aggravated Neurofibromatosis [NCIt concept]
- Ataxia Telangiectasia Syndrome [NCIt concept]
- Neurofibromatosis [NCIt concept]
- Neurofibromatosis Type 1 [NCIt concept]
- Neurofibromatosis Type 1 with Inoperable, Progressive, Symptomatic Plexiform Neurofibromas [NCIt concept]
- Neurofibromatosis Type 2 [NCIt concept]
- Phakomatosis [NCIt concept]
- Recurrent Neurofibromatosis Type 1 [NCIt concept]
- Refractory Neurofibromatosis Type 1 [NCIt concept]
- Sturge-Weber Syndrome [NCIt concept]
- Tuberous Sclerosis [NCIt concept]
- Tuberous Sclerosis 1 [NCIt concept]
- Tuberous Sclerosis 2 [NCIt concept]
- Von Hippel Lindau Syndrome [NCIt concept]
molecular_abnormality_involves_gene
- STK11 Gene [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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