CCPS Disease Terminology

Preferred Label : CCPS Disease Terminology;

NCIt synonyms : Childhood Cancer Predisposition Study Disease Terminology;

NCIt definition : Disease terminology developed to support the activities of the Childhood Cancer Predisposition Study.;

NCI Metathesaurus CUI : CL1643216;

Details

Origin ID

C177516;

UMLS CUI

C5447832;

Semantic type(s)
- Intellectual Product [UMLS semantic type]
subset_includes_concept
- ANKRD26-Related Predisposition to Leukemia and Thrombocytopenia [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 Tumor Predisposition Syndrome [NCIt concept]
- BRCA1/2-Associated Hereditary Breast and Ovarian Cancer Syndrome [NCIt concept]
- Beckwith-Wiedemann Syndrome [NCIt concept]
- Birt-Hogg-Dube Syndrome [NCIt concept]
- Bloom Syndrome [NCIt concept]
- Bohring-Opitz Syndrome [NCIt concept]
- CDC73-Related Neoplastic Syndrome [NCIt concept]
- CDH1-Associated Breast Carcinoma Syndrome [NCIt concept]
- CEPBA-Related Predisposition to Leukemia [NCIt concept]
- CHEK2-Associated Li-Fraumeni-Like Syndrome [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]
- DDX41-Related Predisposition to Leukemia [NCIt concept]
- DICER1 Syndrome [NCIt concept]
- Diamond-Blackfan Anemia [NCIt concept]
- Dyskeratosis Congenita [NCIt concept]
- ETV6-Related Predisposition to Leukemia and Thrombocytopenia [NCIt concept]
- Familial Adenomatous Polyposis [NCIt concept]
- Familial Platelet Disorder with Associated Myeloid Malignancy [NCIt concept]
- Fanconi Anemia [NCIt concept]
- GATA2 Deficiency [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]
- 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]
- Juvenile Polyposis Syndrome [NCIt concept]
- LEOPARD Syndrome [NCIt concept]
- Legius Syndrome [NCIt concept]
- Li-Fraumeni Syndrome [NCIt concept]
- Lymphoproliferative Syndrome 1 [NCIt concept]
- Lynch Syndrome [NCIt concept]
- MIRAGE Syndrome [NCIt concept]
- MUTYH-Associated Polyposis [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]
- 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]
- Oculocutaneous Albinism [NCIt concept]
- PIK3CA-Related Overgrowth Spectrum [NCIt concept]
- Perlman Syndrome [NCIt concept]
- Peutz-Jeghers Syndrome [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]
- SAMD9L-Related Predisposition to Myelodysplastic Syndrome [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]
- Tuberous Sclerosis [NCIt concept]
- Tyrosinemia Type I [NCIt concept]
- Von Hippel Lindau Syndrome [NCIt concept]
- Weaver Syndrome [NCIt concept]
- Wilms Tumor 1 Gene Syndromes [NCIt concept]
- X-Linked Lymphoproliferative Syndrome [NCIt concept]
- Xeroderma Pigmentosum [NCIt concept]

Keyword's position in hierarchy(ies) :

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