PRKAR1A Gene Mutation

Preferred Label : PRKAR1A Gene Mutation;

NCIt definition : A change in the nucleotide sequence of the PRKAR1A gene.;

NCI Metathesaurus CUI : CL512784;

Details

Origin ID

C129503;

UMLS CUI

C4330922;

Molecular abnormality of diseases
- Adult Fibrolamellar Carcinoma [NCIt concept]
- Advanced Fibrolamellar Carcinoma [NCIt concept]
- Carney Complex [NCIt concept]
- Childhood Fibrolamellar Carcinoma [NCIt concept]
- Fibrolamellar Carcinoma [NCIt concept]
- Malignant Melanotic Peripheral Nerve Sheath Tumor [NCIt concept]
- Malignant Melanotic Peripheral Nerve Sheath Tumor of the Mediastinum [NCIt concept]
- Malignant Melanotic Psammomatous Peripheral Nerve Sheath Tumor [NCIt concept]
- Mediastinal Melanotic Schwannoma [NCIt concept]
- Melanotic Schwannoma [NCIt concept]
- Metastatic Fibrolamellar Carcinoma [NCIt concept]
- Recurrent Fibrolamellar Carcinoma [NCIt concept]
- Refractory Fibrolamellar Carcinoma [NCIt concept]
- Testicular Large Cell Calcifying Sertoli Cell Tumor [NCIt concept]
- Unresectable Fibrolamellar Carcinoma [NCIt concept]
Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
molecular_abnormality_involves_gene
- PRKAR1A Gene [NCIt concept]

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