Childhood Cancer Predisposition Study Terminology

Preferred Label : Childhood Cancer Predisposition Study Terminology;

NCIt synonyms : CCPS;

NCIt definition : Terminology developed to support the work of the Childhood Cancer Predisposition Study,;

NCI Metathesaurus CUI : CL1643488;

Details

Origin ID

C177281;

UMLS CUI

C5446142;

Semantic type(s)
- Intellectual Product [UMLS semantic type]
subset_includes_concept
- ACD Gene [NCIt concept]
- ALK Gene [NCIt concept]
- ANKRD26 Gene [NCIt concept]
- ANKRD26-Related Predisposition to Leukemia and Thrombocytopenia [NCIt concept]
- APC Gene [NCIt concept]
- ASXL1 Gene [NCIt concept]
- ATM Gene [NCIt concept]
- ATP7B Gene [NCIt concept]
- Acute Lymphoblastic Leukemia, Susceptibility to, 3 [NCIt concept]
- Ataxia Telangiectasia Syndrome [NCIt concept]
- Ataxia-Pancytopenia Syndrome [NCIt concept]
- Attenuated Familial Adenomatous Polyposis [NCIt concept]
- BAP1 Gene [NCIt concept]
- BAP1 Tumor Predisposition Syndrome [NCIt concept]
- BLM Gene [NCIt concept]
- BMPR1A Gene [NCIt concept]
- BRAF Gene [NCIt concept]
- BRCA1 Gene [NCIt concept]
- BRCA1/2-Associated Hereditary Breast and Ovarian Cancer Syndrome [NCIt concept]
- BRCA2 Gene [NCIt concept]
- BRIP1 Gene [NCIt concept]
- BUB1B Gene [NCIt concept]
- Beckwith-Wiedemann Syndrome [NCIt concept]
- Birt-Hogg-Dube Syndrome [NCIt concept]
- Bloom Syndrome [NCIt concept]
- Bohring-Opitz Syndrome [NCIt concept]
- CBL Gene [NCIt concept]
- CDC73 Gene [NCIt concept]
- CDC73-Related Neoplastic Syndrome [NCIt concept]
- CDH1 Gene [NCIt concept]
- CDH1-Associated Breast Carcinoma Syndrome [NCIt concept]
- CDK4 Gene [NCIt concept]
- CDKN1B Gene [NCIt concept]
- CDKN1C Gene [NCIt concept]
- CDKN2A Gene [NCIt concept]
- CEBPA Gene [NCIt concept]
- CEPBA-Related Predisposition to Leukemia [NCIt concept]
- CHEK2 Gene [NCIt concept]
- CHEK2-Associated Li-Fraumeni-Like Syndrome [NCIt concept]
- CREBBP Gene [NCIt concept]
- CTR9 Gene [NCIt concept]
- Carney Complex [NCIt concept]
- Congenital Amegakaryocytic Thrombocytopenia [NCIt concept]
- Constitutional Mismatch Repair Deficiency Syndrome [NCIt concept]
- Costello Syndrome [NCIt concept]
- Cowden Syndrome [NCIt concept]
- DDB2 Gene [NCIt concept]
- DDX41 Gene [NCIt concept]
- DDX41-Related Predisposition to Leukemia [NCIt concept]
- DICER1 Gene [NCIt concept]
- DICER1 Syndrome [NCIt concept]
- DIS3L2 Gene [NCIt concept]
- DKC1 Gene [NCIt concept]
- Diamond-Blackfan Anemia [NCIt concept]
- Dyskeratosis Congenita [NCIt concept]
- EP300 Gene [NCIt concept]
- EPCAM Gene [NCIt concept]
- ERCC2 Gene [NCIt concept]
- ERCC3 Gene [NCIt concept]
- ERCC4 Gene [NCIt concept]
- ERCC5 Gene [NCIt concept]
- ETV6 Gene [NCIt concept]
- ETV6-Related Predisposition to Leukemia and Thrombocytopenia [NCIt concept]
- EZH2 Gene [NCIt concept]
- FAH Gene [NCIt concept]
- FANCA Gene [NCIt concept]
- FANCB Gene [NCIt concept]
- FANCC Gene [NCIt concept]
- FANCD2 Gene [NCIt concept]
- FANCE Gene [NCIt concept]
- FANCF Gene [NCIt concept]
- FANCG Gene [NCIt concept]
- FANCI Gene [NCIt concept]
- FANCL Gene [NCIt concept]
- FANCM Gene [NCIt concept]
- FBXW7 Gene [NCIt concept]
- FH Gene [NCIt concept]
- FLCN Gene [NCIt concept]
- Familial Adenomatous Polyposis [NCIt concept]
- Familial Platelet Disorder with Associated Myeloid Malignancy [NCIt concept]
- Fanconi Anemia [NCIt concept]
- GATA2 Deficiency [NCIt concept]
- GATA2 Gene [NCIt concept]
- GPC3 Gene [NCIt concept]
- GPC4 Gene [NCIt concept]
- Gain of Chromosome 12q [NCIt concept]
- Gain of Chromosome 15q [NCIt concept]
- Gain of Chromosome 17q [NCIt concept]
- Gain of Chromosome 1q [NCIt concept]
- Gain of Chromosome 20q [NCIt concept]
- Gain of Chromosome 9q [NCIt concept]
- Genetic Predisposition to Melanoma [NCIt concept]
- Genetic Predisposition to Meningioma [NCIt concept]
- Genetic Predisposition to Myofibromatosis [NCIt concept]
- Genetic Predisposition to Neuroblastoma [NCIt concept]
- Genetic Predisposition to Non-Syndromic Wilms Tumor [NCIt concept]
- Genetic Predisposition to Papillary Renal Cell Carcinoma [NCIt concept]
- H19 Gene [NCIt concept]
- HRAS Gene [NCIt concept]
- Hepatolenticular Degeneration [NCIt concept]
- Hereditary Gastrointestinal Stromal Tumor [NCIt concept]
- Hereditary Leiomyomatosis and Renal Cell Carcinoma [NCIt concept]
- Hereditary Paraganglioma-Pheochromocytoma Syndrome [NCIt concept]
- Hereditary Retinoblastoma [NCIt concept]
- IGF2 Gene [NCIt concept]
- ITK Gene [NCIt concept]
- Juvenile Polyposis Syndrome [NCIt concept]
- KCNQ1OT1 Gene [NCIt concept]
- KDM3B Gene [NCIt concept]
- KIT Gene [NCIt concept]
- KRAS Gene [NCIt concept]
- LEOPARD Syndrome [NCIt concept]
- LZTR1 Gene [NCIt concept]
- Legius Syndrome [NCIt concept]
- Li-Fraumeni Syndrome [NCIt concept]
- Loss of Chromosome 13q [NCIt concept]
- Loss of Chromosome 14 [NCIt concept]
- Loss of Chromosome 1p [NCIt concept]
- Loss of Chromosome 22 [NCIt concept]
- Loss of Chromosome 3p [NCIt concept]
- Loss of Chromosome Y [NCIt concept]
- Lymphoproliferative Syndrome 1 [NCIt concept]
- Lynch Syndrome [NCIt concept]
- MAP2K1 Gene [NCIt concept]
- MAPK1 Gene [NCIt concept]
- MAX Gene [NCIt concept]
- MEN1 Gene [NCIt concept]
- MET Gene [NCIt concept]
- MIRAGE Syndrome [NCIt concept]
- MLH1 Gene [NCIt concept]
- MPL Gene [NCIt concept]
- MRAS Gene [NCIt concept]
- MSH2 Gene [NCIt concept]
- MSH6 Gene [NCIt concept]
- MUTYH Gene [NCIt concept]
- MUTYH-Associated Polyposis [NCIt concept]
- Monosomy 7 [NCIt concept]
- Mosaic Variegated Aneuploidy Syndrome 1 [NCIt concept]
- Mulibrey Nanism [NCIt concept]
- Multiple Endocrine Neoplasia Type 1 [NCIt concept]
- Multiple Endocrine Neoplasia Type 2 [NCIt concept]
- Multiple Endocrine Neoplasia Type 4 [NCIt concept]
- NBN Gene [NCIt concept]
- NF1 Gene [NCIt concept]
- NF2 Gene [NCIt concept]
- NHP2 Gene [NCIt concept]
- NOP10 Gene [NCIt concept]
- NOTCH3 Gene [NCIt concept]
- NRAS Gene [NCIt concept]
- NSD1 Gene [NCIt concept]
- NTRK1 Gene [NCIt concept]
- NYNRIN Gene [NCIt concept]
- Neurofibromatosis Type 1 [NCIt concept]
- Neurofibromatosis Type 2 [NCIt concept]
- Nevoid Basal Cell Carcinoma Syndrome [NCIt concept]
- Nijmegen Breakage Syndrome [NCIt concept]
- Noonan Syndrome [NCIt concept]
- Noonan Syndrome-Like Disorder with Loose Anagen Hair [NCIt concept]
- Noonan Syndrome-Like Disorder with or without Juvenile Myelomonocytic Leukemia [NCIt concept]
- OCA2 Gene [NCIt concept]
- OCA5 Gene [NCIt concept]
- OFD1 Gene [NCIt concept]
- Oculocutaneous Albinism [NCIt concept]
- PALB2 Gene [NCIt concept]
- PARN Gene [NCIt concept]
- PAX5 Gene [NCIt concept]
- PDGFRA Gene [NCIt concept]
- PDGFRB Gene [NCIt concept]
- PHOX2B Gene [NCIt concept]
- PIK3CA Gene [NCIt concept]
- PIK3CA-Related Overgrowth Spectrum [NCIt concept]
- PMS2 Gene [NCIt concept]
- POLH Gene [NCIt concept]
- PPP1CB Gene [NCIt concept]
- PRKAR1A Gene [NCIt concept]
- PTCH1 Gene [NCIt concept]
- PTEN Gene [NCIt concept]
- PTPN11 Gene [NCIt concept]
- Perlman Syndrome [NCIt concept]
- Peutz-Jeghers Syndrome [NCIt concept]
- RAD51C Gene [NCIt concept]
- RAF1 Gene [NCIt concept]
- RASA2 Gene [NCIt concept]
- RB1 Gene [NCIt concept]
- RBM8A Gene [NCIt concept]
- RECQL4 Gene [NCIt concept]
- REST Gene [NCIt concept]
- RET Gene [NCIt concept]
- RIT1 Gene [NCIt concept]
- RPL11 Gene [NCIt concept]
- RPL19 Gene [NCIt concept]
- RPL26 Gene [NCIt concept]
- RPL35A Gene [NCIt concept]
- RPL5 Gene [NCIt concept]
- RPS10 Gene [NCIt concept]
- RPS17 Gene [NCIt concept]
- RPS19 Gene [NCIt concept]
- RPS24 Gene [NCIt concept]
- RPS26 Gene [NCIt concept]
- RPS7 Gene [NCIt concept]
- RRAS Gene [NCIt concept]
- RRAS2 Gene [NCIt concept]
- RTEL1 Gene [NCIt concept]
- RUNX1 Gene [NCIt concept]
- Radial Aplasia-Thrombocytopenia Syndrome [NCIt concept]
- Rhabdoid Tumor Predisposition Syndrome 1 [NCIt concept]
- Rhabdoid Tumor Predisposition Syndrome 2 [NCIt concept]
- Rothmund-Thomson Syndrome [NCIt concept]
- Rubinstein-Taybi Syndrome [NCIt concept]
- SAMD9 Gene [NCIt concept]
- SAMD9L Gene [NCIt concept]
- SAMD9L-Related Predisposition to Myelodysplastic Syndrome [NCIt concept]
- SBDS Gene [NCIt concept]
- SDHA Gene [NCIt concept]
- SDHAF2 Gene [NCIt concept]
- SDHB Gene [NCIt concept]
- SDHC Gene [NCIt concept]
- SDHD Gene [NCIt concept]
- SETBP1 Gene [NCIt concept]
- SH2D1A Gene [NCIt concept]
- SHOC2 Gene [NCIt concept]
- SLC24A5 Gene [NCIt concept]
- SLC45A2 Gene [NCIt concept]
- SMAD4 Gene [NCIt concept]
- SMARCA4 Gene [NCIt concept]
- SMARCB1 Gene [NCIt concept]
- SMARCE1 Gene [NCIt concept]
- SOS1 Gene [NCIt concept]
- SOS2 Gene [NCIt concept]
- SPRED1 Gene [NCIt concept]
- STK11 Gene [NCIt concept]
- SUFU Gene [NCIt concept]
- Schinzel-Giedion Midface-Retraction Syndrome [NCIt concept]
- Schwannomatosis [NCIt concept]
- Shwachman-Diamond Syndrome [NCIt concept]
- Simpson-Golabi-Behmel Syndrome [NCIt concept]
- Sotos Syndrome [NCIt concept]
- TERC Gene [NCIt concept]
- TERT Gene [NCIt concept]
- TINF2 Gene [NCIt concept]
- TMEM127 Gene [NCIt concept]
- TP53 Gene [NCIt concept]
- TRIM28 Gene [NCIt concept]
- TRIM37 Gene [NCIt concept]
- TSC1 Gene [NCIt concept]
- TSC2 Gene [NCIt concept]
- TYR Gene [NCIt concept]
- TYRP1 Gene [NCIt concept]
- Trisomy 17 [NCIt concept]
- Trisomy 7 [NCIt concept]
- Tuberous Sclerosis [NCIt concept]
- Tyrosinemia Type I [NCIt concept]
- VHL Gene [NCIt concept]
- Von Hippel Lindau Syndrome [NCIt concept]
- WRAP53 Gene [NCIt concept]
- WT1 Gene [NCIt concept]
- Weaver Syndrome [NCIt concept]
- Wilms Tumor 1 Gene Syndromes [NCIt concept]
- X-Linked Lymphoproliferative Syndrome [NCIt concept]
- XIAP Gene [NCIt concept]
- XPA Gene [NCIt concept]
- XPC Gene [NCIt concept]
- Xeroderma Pigmentosum [NCIt concept]
- del(11p15.5) [NCIt concept]
- del(9p21) [NCIt concept]

Keyword's position in hierarchy(ies) :

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