Atlas of Genetics and Cytogenetics in Oncology and Haematology


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List of cancer prone diseases

Updated : Thu Aug 14 09:30:51 2008


SymbolCollaboration
Aicardi syndrome / Agenesis of corpus callosum with chorioretinal abnormalityFOR_SALE
Alagille syndrome (AGS)DONE
AlbinismFOR_SALE
Aplasia cutis congenita with epibulbar dermoids/ Oculoectodermal syndromeFOR_SALE
Ataxia telangiectasiaDONE
Autoimmune Lymphoproliferative SyndromeDONE
Bannayan-Riley-Ruvalcaba syndromeDONE
Bazex syndrome / Follicular atrophoderma and basal cell carcinomasFOR_SALE
Beckwith-Wiedemann syndromeDONE
Birt-Hogg-Dubé Syndrome (BHD)DONE
Bloom syndromeDONE
Bruton's agammaglobulinemiaDONE
Carney complex (CNC)DONE
Carney triad / Gastric leiomyosarcoma, pulmonary chondroma, and extraadrenal paragangliomaFOR_SALE
Cartilage-hair hypoplasia (CHH)DONE
Chediak-Higashi syndromeFOR_SALE
Cockayne syndromeDONE
Common variable immunodeficiencyreserved
Congenital MyofibromatosisDONE
Congenital central hypoventilation syndrome and tumors of the sympathetic nervous systemFOR_SALE
Congenital neutropeniaDONE
Costello syndromeDONE
Cowden DiseaseDONE
Currarino SyndromeDONE
Cutaneous malignant melanoma 2 (CMM2)FOR_SALE
De Sanctis-Cacchione syndromeFOR_SALE
Denys-Drashreserved
Diamond-Blackfan anemia (DBA)DONE
Dianzani Autoimmune Lymphoproliferative Disease (DALD)DONE
Diaphyseal Medullary Stenosis with Malignant Fibrous Histiocytoma (DMS-MFH)DONE
Dubowitz syndromeDONE
Dyskeratosis congenita (DKC)DONE
Dysplastic nevus syndrome (DNS)DONE
Epidermodysplasia verruciformisDONE
Esophageal and vulval leiomyomatosis with nephropathy / Alport syndrome and diffuse leiomyomatosisFOR_SALE
Familial (Hereditary) diffuse type gastric cancer    FOR_SALE
Familial /sporadic gastrointestinal stromal tumors (GISTs)DONE
Familial Atypical Multiple Mole Melanoma (FAMMM)FOR_SALE
Familial Chronic Lymphocytic LeukaemiaDONE
Familial Monosomy 7 SyndromeDONE
Familial adenomatous polyposis (FAP)DONE
Familial chordomareserved
Familial clear cell renal cancerDONE
Familial cylindromatosis / Turban tumor syndrome / Dermal eccrine cylindromasFOR_SALE
Familial ependymomaFOR_SALE
Familial liver adenomatosisDONE
Familial melanomaDONE
Familial nervous system tumour syndromesDONE
Familial neuroblastomaFOR_SALE
Familial platelet disorder with predisposition to acute leukemiareserved
Familial platelet storage pool deficiencyreserved
Familial thymoma / familial thymic neoplasiareserved
Familial thyroglossal duct cystFOR_SALE
Familial tylosis oesophageal cancer / Keratosis palmaris et plantaris with esophageal cancerFOR_SALE
Fanconi anaemiaDONE
Generalised basaloid follicular hamartoma syndromeFOR_SALE
Glomuvenous malformation (GVM)DONE
Hemihyperplasia isolatedDONE
Hereditary Desmoid Disease.DONE
Hereditary Pancreatic CancerDONE
Hereditary Paraganglioma (PGL)DONE
Hereditary adrenocortical carcinomaFOR_SALE
Hereditary breast cancerDONE
Hereditary kidney cancerFOR_SALE
Hereditary leiomyomatosis and renal cell cancerFOR_SALE
Hereditary medullary thyroid carcinomaFOR_SALE
Hereditary multiple leiomyoma of skin / Multiple cutaneous and uterine leiomyomata 1FOR_SALE
Hereditary non polyposis colorectal carcinoma (HNPCC Syndrome)DONE
Hereditary ovarian cancerFOR_SALE
Hereditary pancreatitisFOR_SALE
Hereditary papillary renal cell carcinomaDONE
Hereditary prostate cancerDONE
Holoprosencephaly-Diencephalic Hamartoblastoma (HDH).DONE
Hyperparathyroidism-Jaw Tumor syndrome (HPT-JT)DONE
Ichthyosis, X-linked / Steroid sulfatase deficiency diseaseFOR_SALE
Isolated mucocutaneous melanotic pigmentationFOR_SALE
Juvenile hyaline fibromatosis / puretic syndromeFOR_SALE
Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome consiste en :juv. Polyp. (VOIR ATLAS 10047: OMIM 174900) + hered. hem. telang.FOR_SALE
Klippel Trenaunay SyndromeDONE
LEOPARD syndromeDONE
Lhermitte-Duclos diseaseDONE
Li-Fraumeni SyndromeDONE
MAP (MUTYH-Associated Polyposis )DONE
MUTYH associated polyposisDONE
McCune Albright SyndromeDONE
Melanoma-Astrocytoma syndromeDONE
Muir-Torre syndromeFOR_SALE
Mulibrey nanism / Muscle-liver-brain-eye nanism / Pericardial constriction and growth failure / Perheentupa syndromeFOR_SALE
Multiple Endocrine Neoplasia type 1 (MEN1)DONE
Multiple Endocrine Neoplasia type 2 (MEN2)DONE
Multiple Osteochondromas (MO)DONE
Multiple familial trichoepithelioma / Epithelioma adenoides cysticum of Brooke / Hereditary multiple benign cystic pitheliomaFOR_SALE
Multiple self healing squam epitheliomaFOR_SALE
Naevoid basal cell carcinoma syndrome (NBCS)DONE
Neuroectodermal tumors, supratentorial primitive, with cafe-au-lait spotsreserved
Neurofibromatosis type 1 (NF1)DONE
Neurofibromatosis type 2 (NF2)DONE
Nijmegen breakage syndromeDONE
Noonan syndromeDONE
Oligodontia-colorectal cancer syndrome / Tooth agenesis-colorectal cancer syndromeFOR_SALE
Overgrowth, Lipomatosis and truncated HMGA2reserved
Pallister Hall Syndrome (PHS)DONE
Perlman syndrome (renal hamartomas, nephroblastomatosis and fetal gigantism)DONE
Peutz-Jeghers syndromeDONE
Pheochromocytoma--islet cell tumor syndromeFOR_SALE
PiebaldismDONE
Porokeratosis of MibelliDONE
Prader Willi SyndromeDONE
Progressive osseous heteroplasia / Familial ectopic ossification / Osteoma cutislater
Proteus SyndromeDONE
RetinoblastomaDONE
Rhabdoid predisposition syndromeDONE
Rothmund-Thomson syndrome (RTS)DONE
Rubinstein-Taybi syndrome (RTS)DONE
Schinzel-Giedion midface retraction syndromeDONE
Schopf-Schulz-Passarge syndrome / keratosis palmoplantaris with cystic eyelids, hypodontia, and hypotrichosis / Eccrine tumors with ectodermal dysplasiareserved
SchwannomatosisDONE
Second breast cancer syndrome (BRCA2)FOR_SALE
Shwachman-Diamond Syndrome (SDS)DONE
Simpson-Golabi-Behmel SyndromeDONE
Sjogren syndrome (Gougerot-Sjogren syndrome)FOR_SALE
Sotos syndromeDONE
Spiegler-Brooke syndrome / Ancell-Spiegler cylindromasFOR_SALE
Stiff-person syndromeDONE
Sturge Weber syndromeDONE
Susceptibility to ulcerative colitisFOR_SALE
Trichothiodystrophy (TTD)DONE
Trisomy 21 (constit)reserved
Trisomy 8 (constit)reserved
Tuberous Sclerosis (TSC)DONE
Turcot syndromeDONE
Variegated aneuploidy related to premature centromere division (PCD)DONE
Von Hippel-LindauDONE
WAGR (Wilms' tumor/aniridia/genitourinary anomalies/mental retardation syndrome)DONE
Waardenburg syndrome (WS)DONE
Weaver syndromeDONE
Werner syndromeDONE
Wiskott-Aldrich syndromeFOR_SALE
X-linked Iymphoproliferative syndromeFOR_SALE
Xeroderma pigmentosumDONE
familial juvenile polyposisFOR_SALE
predisposition to endometrial carcinomaFOR_SALE


Please contact
Jean-Loup Huret, Genetics University Hospital
F-86021 POITIERS FRANCE
email : j.l.huret@chu-poitiers.fr.
tel +33 5 49 44 45 46
fax +33 5 49 44 41 31 (or... 39 80)


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