List of cancer prone diseases |
Updated : Thu Aug 14 09:30:51 2008
| Symbol | Collaboration |
|---|---|
| Aicardi syndrome / Agenesis of corpus callosum with chorioretinal abnormality | FOR_SALE |
| Alagille syndrome (AGS) | DONE |
| Albinism | FOR_SALE |
| Aplasia cutis congenita with epibulbar dermoids/ Oculoectodermal syndrome | FOR_SALE |
| Ataxia telangiectasia | DONE |
| Autoimmune Lymphoproliferative Syndrome | DONE |
| Bannayan-Riley-Ruvalcaba syndrome | DONE |
| Bazex syndrome / Follicular atrophoderma and basal cell carcinomas | FOR_SALE |
| Beckwith-Wiedemann syndrome | DONE |
| Birt-Hogg-Dubé Syndrome (BHD) | DONE |
| Bloom syndrome | DONE |
| Bruton's agammaglobulinemia | DONE |
| Carney complex (CNC) | DONE |
| Carney triad / Gastric leiomyosarcoma, pulmonary chondroma, and extraadrenal paraganglioma | FOR_SALE |
| Cartilage-hair hypoplasia (CHH) | DONE |
| Chediak-Higashi syndrome | FOR_SALE |
| Cockayne syndrome | DONE |
| Common variable immunodeficiency | reserved |
| Congenital Myofibromatosis | DONE |
| Congenital central hypoventilation syndrome and tumors of the sympathetic nervous system | FOR_SALE |
| Congenital neutropenia | DONE |
| Costello syndrome | DONE |
| Cowden Disease | DONE |
| Currarino Syndrome | DONE |
| Cutaneous malignant melanoma 2 (CMM2) | FOR_SALE |
| De Sanctis-Cacchione syndrome | FOR_SALE |
| Denys-Drash | reserved |
| Diamond-Blackfan anemia (DBA) | DONE |
| Dianzani Autoimmune Lymphoproliferative Disease (DALD) | DONE |
| Diaphyseal Medullary Stenosis with Malignant Fibrous Histiocytoma (DMS-MFH) | DONE |
| Dubowitz syndrome | DONE |
| Dyskeratosis congenita (DKC) | DONE |
| Dysplastic nevus syndrome (DNS) | DONE |
| Epidermodysplasia verruciformis | DONE |
| Esophageal and vulval leiomyomatosis with nephropathy / Alport syndrome and diffuse leiomyomatosis | FOR_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 Leukaemia | DONE |
| Familial Monosomy 7 Syndrome | DONE |
| Familial adenomatous polyposis (FAP) | DONE |
| Familial chordoma | reserved |
| Familial clear cell renal cancer | DONE |
| Familial cylindromatosis / Turban tumor syndrome / Dermal eccrine cylindromas | FOR_SALE |
| Familial ependymoma | FOR_SALE |
| Familial liver adenomatosis | DONE |
| Familial melanoma | DONE |
| Familial nervous system tumour syndromes | DONE |
| Familial neuroblastoma | FOR_SALE |
| Familial platelet disorder with predisposition to acute leukemia | reserved |
| Familial platelet storage pool deficiency | reserved |
| Familial thymoma / familial thymic neoplasia | reserved |
| Familial thyroglossal duct cyst | FOR_SALE |
| Familial tylosis oesophageal cancer / Keratosis palmaris et plantaris with esophageal cancer | FOR_SALE |
| Fanconi anaemia | DONE |
| Generalised basaloid follicular hamartoma syndrome | FOR_SALE |
| Glomuvenous malformation (GVM) | DONE |
| Hemihyperplasia isolated | DONE |
| Hereditary Desmoid Disease. | DONE |
| Hereditary Pancreatic Cancer | DONE |
| Hereditary Paraganglioma (PGL) | DONE |
| Hereditary adrenocortical carcinoma | FOR_SALE |
| Hereditary breast cancer | DONE |
| Hereditary kidney cancer | FOR_SALE |
| Hereditary leiomyomatosis and renal cell cancer | FOR_SALE |
| Hereditary medullary thyroid carcinoma | FOR_SALE |
| Hereditary multiple leiomyoma of skin / Multiple cutaneous and uterine leiomyomata 1 | FOR_SALE |
| Hereditary non polyposis colorectal carcinoma (HNPCC Syndrome) | DONE |
| Hereditary ovarian cancer | FOR_SALE |
| Hereditary pancreatitis | FOR_SALE |
| Hereditary papillary renal cell carcinoma | DONE |
| Hereditary prostate cancer | DONE |
| Holoprosencephaly-Diencephalic Hamartoblastoma (HDH). | DONE |
| Hyperparathyroidism-Jaw Tumor syndrome (HPT-JT) | DONE |
| Ichthyosis, X-linked / Steroid sulfatase deficiency disease | FOR_SALE |
| Isolated mucocutaneous melanotic pigmentation | FOR_SALE |
| Juvenile hyaline fibromatosis / puretic syndrome | FOR_SALE |
| Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome consiste en :juv. Polyp. (VOIR ATLAS 10047: OMIM 174900) + hered. hem. telang. | FOR_SALE |
| Klippel Trenaunay Syndrome | DONE |
| LEOPARD syndrome | DONE |
| Lhermitte-Duclos disease | DONE |
| Li-Fraumeni Syndrome | DONE |
| MAP (MUTYH-Associated Polyposis ) | DONE |
| MUTYH associated polyposis | DONE |
| McCune Albright Syndrome | DONE |
| Melanoma-Astrocytoma syndrome | DONE |
| Muir-Torre syndrome | FOR_SALE |
| Mulibrey nanism / Muscle-liver-brain-eye nanism / Pericardial constriction and growth failure / Perheentupa syndrome | FOR_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 pithelioma | FOR_SALE |
| Multiple self healing squam epithelioma | FOR_SALE |
| Naevoid basal cell carcinoma syndrome (NBCS) | DONE |
| Neuroectodermal tumors, supratentorial primitive, with cafe-au-lait spots | reserved |
| Neurofibromatosis type 1 (NF1) | DONE |
| Neurofibromatosis type 2 (NF2) | DONE |
| Nijmegen breakage syndrome | DONE |
| Noonan syndrome | DONE |
| Oligodontia-colorectal cancer syndrome / Tooth agenesis-colorectal cancer syndrome | FOR_SALE |
| Overgrowth, Lipomatosis and truncated HMGA2 | reserved |
| Pallister Hall Syndrome (PHS) | DONE |
| Perlman syndrome (renal hamartomas, nephroblastomatosis and fetal gigantism) | DONE |
| Peutz-Jeghers syndrome | DONE |
| Pheochromocytoma--islet cell tumor syndrome | FOR_SALE |
| Piebaldism | DONE |
| Porokeratosis of Mibelli | DONE |
| Prader Willi Syndrome | DONE |
| Progressive osseous heteroplasia / Familial ectopic ossification / Osteoma cutis | later |
| Proteus Syndrome | DONE |
| Retinoblastoma | DONE |
| Rhabdoid predisposition syndrome | DONE |
| Rothmund-Thomson syndrome (RTS) | DONE |
| Rubinstein-Taybi syndrome (RTS) | DONE |
| Schinzel-Giedion midface retraction syndrome | DONE |
| Schopf-Schulz-Passarge syndrome / keratosis palmoplantaris with cystic eyelids, hypodontia, and hypotrichosis / Eccrine tumors with ectodermal dysplasia | reserved |
| Schwannomatosis | DONE |
| Second breast cancer syndrome (BRCA2) | FOR_SALE |
| Shwachman-Diamond Syndrome (SDS) | DONE |
| Simpson-Golabi-Behmel Syndrome | DONE |
| Sjogren syndrome (Gougerot-Sjogren syndrome) | FOR_SALE |
| Sotos syndrome | DONE |
| Spiegler-Brooke syndrome / Ancell-Spiegler cylindromas | FOR_SALE |
| Stiff-person syndrome | DONE |
| Sturge Weber syndrome | DONE |
| Susceptibility to ulcerative colitis | FOR_SALE |
| Trichothiodystrophy (TTD) | DONE |
| Trisomy 21 (constit) | reserved |
| Trisomy 8 (constit) | reserved |
| Tuberous Sclerosis (TSC) | DONE |
| Turcot syndrome | DONE |
| Variegated aneuploidy related to premature centromere division (PCD) | DONE |
| Von Hippel-Lindau | DONE |
| WAGR (Wilms' tumor/aniridia/genitourinary anomalies/mental retardation syndrome) | DONE |
| Waardenburg syndrome (WS) | DONE |
| Weaver syndrome | DONE |
| Werner syndrome | DONE |
| Wiskott-Aldrich syndrome | FOR_SALE |
| X-linked Iymphoproliferative syndrome | FOR_SALE |
| Xeroderma pigmentosum | DONE |
| familial juvenile polyposis | FOR_SALE |
| predisposition to endometrial carcinoma | FOR_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)