Información:
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ID
5446
Descripción
Genetische und immunologische Charakterisierung der schweren aplastischen Anaemie (SAA) bei Kindern und Jugendlichen (EWOG-SAA) http://ewog-mds.org/
Link
Palabras clave
Versiones (1)
- 6/8/14 6/8/14 - Martin Dugas
Subido en
6 de agosto de 2014
DOI
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Licencia
Creative Commons BY-NC 3.0 Legacy
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EWOG SAA Data on HSCT patient
Data on HSCT patient
- StudyEvent: SE
Similar models
Data on HSCT patient
- StudyEvent: SE
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Dummy
Item
Dummy
text
CL Item
No (1)
CL Item
Yes (2)
CL Item
No (1)
CL Item
Yes (2)
CL Item
No (1)
CL Item
Yes (2)
CL Item
No (1)
CL Item
Yes (2)
Date of diagnosis
Item
Date of diagnosis
date
CL Item
Acute leukemia (1000000)
CL Item
Chronic leukemia (2000000)
CL Item
Lymphoma (3000000)
CL Item
Plasma cell disorder (4000000)
CL Item
Solid tumour (5000000)
CL Item
Myelodysplastic / Myeloproliferative syndrome (6000000)
CL Item
Bone marrow failure including aplastic anaemia (7000000)
CL Item
Inherited disorder (8000000)
CL Item
Histiocytic disorder (9000000)
CL Item
Autoimmune disorder (10000000)
CL Item
Haemoglobinopathy (11000000)
CL Item
AML (1001000)
CL Item
ALL (1002000)
CL Item
CML (2001000)
CL Item
CLL (2002000)
CL Item
PPL (2003000)
CL Item
NHL (3001000)
CL Item
Hodgkin (3002000)
CL Item
Multiple myeloma (4001000)
CL Item
Plasma cell leukemia (4002001)
CL Item
Solitary plasmacytoma (4003001)
CL Item
Primary amyloidosis (4004001)
CL Item
Bone sarcoma (excluding EWING/PNET) (5010001)
CL Item
Osteosarcoma (5011001)
CL Item
Chondrosarcoma (5012001)
CL Item
Astrocytoma (5021001)
CL Item
Oligodendroglioma (5022001)
CL Item
Glioblastoma (5023001)
CL Item
Ependymoma (5024001)
CL Item
Other glioma (5025001)
CL Item
PNET (5030001)
CL Item
Ewing sarcoma (5031001)
CL Item
Medulloblastoma (5032001)
CL Item
Neuroblastoma (5033001)
CL Item
Central nervous system (including CNS PNET) (5034001)
CL Item
Retinoblastoma (5036001)
CL Item
Ewing sarcoma/PNET, extra-skeletal (5037001)
CL Item
Ewing sarcoma/PNET, skeletal (5038001)
CL Item
Germ cell tumour (5040001)
CL Item
Seminoma (5041001)
CL Item
Embryonal carcinoma (5042001)
CL Item
Teratocarcinoma (yolk sac tumour) (5043001)
CL Item
Testicular (5044001)
CL Item
Germ cell tumour, extragonadal (5045001)
CL Item
Choriocarcinoma (5046001)
CL Item
Mixed tumour without seminoma (5047001)
CL Item
Mixed tumour with seminoma (5048001)
CL Item
Ovarian (5049001)
CL Item
Skin tumour (5050001)
CL Item
Melanoma (5051001)
CL Item
Lung, unspecified (5053001)
CL Item
Small cell lung cancer (SCLC) (5054001)
CL Item
Non-small cell lung cancer (NSCLC) (5057001)
CL Item
Soft tissue sarcoma (5060001)
CL Item
Myxoma (5061001)
CL Item
Mesenchymoma (5062001)
CL Item
Leiomyiosarcoma (5063001)
CL Item
Rhabdomyiosarcoma (5064001)
CL Item
Liposarcoma (5065001)
CL Item
Fibrosarcoma (5066001)
CL Item
Synovial sarcoma (5067001)
CL Item
Angiosarcoma (5068001)
CL Item
Haemangiosarcoma (5069001)
CL Item
Lymphangiosarcoma (5070001)
CL Item
Neurogenic sarcoma (5071001)
CL Item
Hepatobiliary (5072001)
CL Item
Pancreas (5074001)
CL Item
Prostate (5075001)
CL Item
Breast (5080000)
CL Item
Undifferentiated carcinoma (5090001)
CL Item
Thymoma (5091001)
CL Item
Gastric carcinoma + adenocarcinoma (5092001)
CL Item
Adenocarcinoma origin X (5093001)
CL Item
Colon adenocarcinoma (5096001)
CL Item
Granulocytic sarcoma (5097001)
CL Item
Wilms tumour (5098001)
CL Item
Other kidney tumour (5099001)
CL Item
Other solid tumour (5777001)
CL Item
Unknown solid tumour (5999001)
CL Item
MDS (6001000)
CL Item
MPS (6002000)
CL Item
MDS and MPS combined (6003000)
CL Item
Other myelodysplatic syndrome (6004001)
CL Item
Non constitutional (7001000)
CL Item
Fanconi (congenital) (7002001)
CL Item
Pure red cell aplasia (non congenital PRCA) (7003000)
CL Item
Diamond-Blackfan (congenital PRCA) (7004001)
CL Item
Paroxysmal nocturnal haemoglobinuria (PNH) (7005000)
CL Item
Amegakariocytic thrombocytopaenia (not congenital) (7006000)
CL Item
Schwachman-Diamond (congenital) (7007001)
CL Item
Primaryimmune deficiency (8001000)
CL Item
Disorders of metabolism (8002000)
CL Item
Other inherited disorder (8003000)
CL Item
Familial erythro/hemophagocytic lymphohistiocytosis (9001001)
CL Item
Langerhans cell histiocytosis (Histiocytosis-X) (9002001)
CL Item
Hemophagocytosis (reactive or viral associated) (9003001)
CL Item
Malignant histiocytosis (9004001)
CL Item
Other histiocytic disorder (9077001)
CL Item
Unknown histiocytic disorder (9099001)
CL Item
Connective tissue disease (10001000)
CL Item
Vasculitis (10002000)
CL Item
Arthristis (10003000)
CL Item
Multiple sclerosis (10004001)
CL Item
Other neurological (10005000)
CL Item
Haematological (10006000)
CL Item
Bowel disease (10007000)
CL Item
Other autoimmune disorder (10077001)
CL Item
Precursor B-cell ALL (1002001)
CL Item
t(9;22)(a34;q11) BCR/ABL (1002002)
CL Item
t(v;11q23) MLL rearranged (1002003)
CL Item
t(1;19)(q23;p13) E2A/PBX1 (1002004)
CL Item
t(12;21)(p12;q22) ETV/CBF-alpha (1002005)
CL Item
Precursor T-cell ALL (1002011)
CL Item
ALL not otherwise specified or other (1002077)
CL Item
Unknown ALL (1002099)
CL Item
AML w t(8;21)(q22;q22), (AML1/ETO) (1001001)
CL Item
AML w abnormal BM eosinophils und inv(16)(p13;q22) (1001002)
CL Item
AML w t(15;17)(q22;q12), (PML/RARalpha) [M3] (1001003)
CL Item
AML w 11q23, (MLL) abnormalities (1001004)
CL Item
AML w multilineage dysplasia (w/o MDS or MP/MDS) (1001005)
CL Item
AML not otherwise categorised (1001009)
CL Item
AML mimimally differentiated [M0] (1001010)
CL Item
AML wo maturation [M1] (1001011)
CL Item
AML w maturation [M2] (1001012)
CL Item
Acute myelomonocytic leukemia [M4] (1001014)
CL Item
Acute monoblastic/monocytic leukemia [M5] (1001015)
CL Item
Acute erythroid leukemia [M6] (1001016)
CL Item
Acute megakaryoblastic leukemia [M7] (1001017)
CL Item
Acute basophilic leukemia (1001018)
CL Item
Acute panmyelosis with myelofibrosis (1001019)
CL Item
Myeloid sarcoma (1001020)
CL Item
AML not otherwise specified or other (1001777)
CL Item
Unknown AML (1001999)
CL Item
(t9) (2001001)
CL Item
(t9;22) positive (2001002)
CL Item
Other chromosome abnormality (2001003)
CL Item
Other CML (2001077)
CL Item
Unknown CML (2001099)
CL Item
CLL B-cell/Small lymphocytic lymphoma (2002001)
CL Item
CLL T-cell (2002002)
CL Item
Hairy cell leukaemia (2002003)
CL Item
Atypic hairy cell leukaemia (2002004)
CL Item
Richters syndrome (2002005)
CL Item
Other leukemia (2002077)
CL Item
Unknown leukaemia (2002099)
CL Item
PPL B-cell (2003001)
CL Item
PPL T-cell (2003002)
CL Item
Other PPL (2003077)
CL Item
Unknown PPL (2003099)
CL Item
NHL unspecified (3001001)
CL Item
B-cell NHL unspecified (3001005)
CL Item
Follicular (3001010)
CL Item
Mantle cell (3001020)
CL Item
Extranodal marginal zone B-cell of MALT type (3001030)
CL Item
Diffuse large B-cell (3001040)
CL Item
Centroblastic (3001041)
CL Item
Immunoblastic (3001042)
CL Item
Anaplastic large B-cell (3001043)
CL Item
Intravascular large cell lymphoma (3001045)
CL Item
Mediastinal large cell lymphoma (3001046)
CL Item
Primary effusion large cell lymphoma (3001047)
CL Item
Burkitts lymphoma/Burkitt cell leukaemia (3001050)
CL Item
High grade B-cell lymphoma, Burkitt-like (prov.) (3001051)
CL Item
Precursor B-cell lymphoblastic (3001060)
CL Item
Lymphoplasmcytic lymphoma including Waldenstrom (3001070)
CL Item
Lymphoplasmcytic lymphoma (3001071)
CL Item
Waldenstrom macroglobulinaemia (3001072)
CL Item
Splenic marginal zone (3001080)
CL Item
Nodal marginal zone (3001090)
CL Item
Primary CNS lymphoma (3001096)
CL Item
T-cell NHL unspecified (3001105)
CL Item
Angioimmunoblastic T-cell (AILD) (3001110)
CL Item
Peripheral T-cell (3001120)
CL Item
Anaplastic large T-cell (3001130)
CL Item
Anaplastic large-cell, T/null-cell, primary cuta (3001131)
CL Item
Anaplastic large-cell T/null-cell, primary syste (3001132)
CL Item
PreT lymphoblastic (3001140)
CL Item
Blast NK cell (3001145)
CL Item
Extranodal NK/T-cell (3001150)
CL Item
Enteropathy type T-cell (3001160)
CL Item
Hepatosplenic gamma-delta T-cell (3001170)
CL Item
Subcutaneous panniculitis-like T-cell (3001180)
CL Item
Adult T-cell lymphoma/leukaemia (3001181)
CL Item
Aggressive NK-cell leukaemia (3001182)
CL Item
Large T-cell granular lymphocytic leukaemia (3001183)
CL Item
Mycosis fungoides (3001190)
CL Item
Sezary syndrome (3001195)
CL Item
Post-transplant lymphoproliferative disease (PTL (3001300)
CL Item
Other NHL (3001800)
CL Item
Unknown NHL (3001999)
CL Item
Nodular lymphocyte predominant (3002001)
CL Item
Lymphocyte rich (3002002)
CL Item
Nodular sclerosis (3002003)
CL Item
Mixed cellularity (3002004)
CL Item
Lymphoma depleted (3002005)
CL Item
Other Hodgkin lymphoma (3002077)
CL Item
Unknown Hodgkin lymphoma (3002099)
CL Item
Multiple myeloma light chain (4001001)
CL Item
Multiple myeloma light chain kappa (4001002)
CL Item
Multiple myeloma light chain lambda (4001003)
CL Item
Multiple myeloma light chain both (4001004)
CL Item
Multiple myeloma light chain unknown (4001005)
CL Item
Multiple myeloma non secretory (4001006)
CL Item
Multiple myeloma non secretory stage I (4001007)
CL Item
Multiple myeloma non secretory stage II (4001008)
CL Item
Multiple myeloma non secretory stage III (4001009)
CL Item
Multiple myeloma not evaluated (4001010)
CL Item
Multiple myeloma unknown (4001011)
CL Item
Multiple myeloma common type IgG (4001012)
CL Item
Multiple myeloma common type IgA (4001013)
CL Item
Multiple myeloma common type IgD (4001014)
CL Item
Multiple myeloma common type IgE (4001015)
CL Item
Multiple myeloma common type IgM (4001016)
CL Item
Multiple myeloma common type unknown (4001017)
CL Item
Breast cancer M0 (No distant metastasis) (5080010)
CL Item
Breast cancer M1 (With distant metastasis) (5080011)
CL Item
Breast cancer MX (Distant metastasis not evaluable) (5080015)
CL Item
Breast cancer not evaluated (5080088)
CL Item
Breast cancer unknown (5080099)
CL Item
MDS RA (6001001)
CL Item
MDS RARS (6001002)
CL Item
MDS RAEB-1 (6001003)
CL Item
MDS RAEB-2 (6001004)
CL Item
MDS Refractory cytopenia with multilineage dysplasia (6001005)
CL Item
MDS RCMD-RS (6001006)
CL Item
MDS associated with isolated del(5q) (6001007)
CL Item
MDS Transformed to AML (6001008)
CL Item
MDS Unclassifiable (MDS-U) or other (6001077)
CL Item
MDS unknown (6001099)
CL Item
MPS Chronic idiopathic myelofibrosis (primary) (6002001)
CL Item
MPS Polycythemia vera (6002002)
CL Item
MPS Essential or primary thrombocythemia (6002003)
CL Item
MPS Hyper eosinophilic syndrome (HES) (6002004)
CL Item
MPS Chronic eosinophilic leukaemia (CEL) (6002005)
CL Item
MPS Chronic neutrophilic leukaemia (6002006)
CL Item
MPS Stem cell leuk-lymphoma syndrome (8p11 syndr) (6002007)
CL Item
MPS Secondary myelofibrosis (6002008)
CL Item
MPS Transformed to AML (6002009)
CL Item
MPS Systemic mastocytosis (6002010)
CL Item
MPS not otherwise specified or other (6002077)
CL Item
MPS unknown (6002099)
CL Item
Chronic myelomonocytic leukaemia (6003001)
CL Item
Juvenile myelomonocytic leukaemia (6003002)
CL Item
Atypical CML (t(9;22) and bcr-abl negative (6003003)
CL Item
MDS and MPS combined other (6003077)
CL Item
MDS and MPS combined unknown (6003099)
Item
Subclassification of non constitutional anaemia
text
Code List
Subclassification of non constitutional anaemia
CL Item
Non constitutional anaemia idiopathic (7001010)
CL Item
Non constitutional anaemia congenital (7001020)
CL Item
Non constitutional anaemia post-hepatic (7001030)
CL Item
Non constitutional anaemia post-hepat A (7001031)
CL Item
Non constitutional anaemia post-hepat B (7001032)
CL Item
Non constitutional anaemia postHep noAB (7001033)
CL Item
Non constitutional anaemia drug related (7001040)
CL Item
Non constitutional anaemia toxic (7001050)
CL Item
Non constitutional anaemia other viral (7001060)
CL Item
Non constitutional anaemia other (7001077)
CL Item
Non constitutional anaemia unknown (7001099)
CL Item
PRCA idiopathic (7003010)
CL Item
PRCA congenital (7003020)
CL Item
PRCA post-hepatic (7003030)
CL Item
PRCA post-hepat A (7003031)
CL Item
PRCA post-hepat B (7003032)
CL Item
PRCA postHep noAB (7003033)
CL Item
PRCA drug related (7003040)
CL Item
PRCA toxic (7003050)
CL Item
PRCA other viral (7003060)
CL Item
PRCA other (7003077)
CL Item
PRCA unknown (7003099)
CL Item
PNH idiopathic (7005010)
CL Item
PNH congenital (7005020)
CL Item
PNH post-hepatic (7005030)
CL Item
PNH post-hepat A (7005031)
CL Item
PNH post-hepat B (7005032)
CL Item
PNH postHep noAB (7005033)
CL Item
PNH drug related (7005040)
CL Item
PNH toxic (7005050)
CL Item
PNH other viral (7005060)
CL Item
PNH other (7005077)
CL Item
PNH unknown (7005099)
Item
Subclassification of amegakariocytic thrombocytopaenia (not congenital)
text
Code List
Subclassification of amegakariocytic thrombocytopaenia (not congenital)
CL Item
Amegakariocytic thrombocytopaenia (not congenital) Idiopathic (7006010)
CL Item
Amegakariocytic thrombocytopaenia (not congenital) Congenital (7006020)
CL Item
Amegakariocytic thrombocytopaenia (not congenital) Post-hepatic (7006030)
CL Item
Amegakariocytic thrombocytopaenia (not congenital) Post-hepat A (7006031)
CL Item
Amegakariocytic thrombocytopaenia (not congenital) Post-hepat B (7006032)
CL Item
Amegakariocytic thrombocytopaenia (not congenital) PostHep noAB (7006033)
CL Item
Amegakariocytic thrombocytopaenia (not congenital) Drug related (7006040)
CL Item
Amegakariocytic thrombocytopaenia (not congenital) Toxic (7006050)
CL Item
Amegakariocytic thrombocytopaenia (not congenital) Other viral (7006060)
CL Item
Amegakariocytic thrombocytopaenia (not congenital) Other (7006077)
CL Item
Amegakariocytic thrombocytopaenia (not congenital) unknown (7006099)
Item
Subclassification of primaryimmune deficiency
text
CL Item
Absence of T and B cells SCID (8001010)
CL Item
Artemis (8001011)
CL Item
Ligase IV (8001012)
CL Item
Rag-1 or Rag-2 (8001013)
CL Item
Other T- B- cells SCID (8001017)
CL Item
Absence of T, normal B cell SCID (8001020)
CL Item
Gamma c deficiency (8001021)
CL Item
JAK 3 deficiency (8001022)
CL Item
IL-7R alpha deficiency (8001023)
CL Item
Other T- B+ cells SCID (8001027)
CL Item
ADA deficiency (Adenosine deaminase deficiency) (8001031)
CL Item
Purine nucleoside phosphorylase deficiency (PNP- (8001032)
CL Item
Reticular dysgenesis (AR) (8001033)
CL Item
Other SCID (8001037)
CL Item
Combined immune deficiency (CID), unspecified (8001050)
CL Item
Omenn syndrome (8001051)
CL Item
Neutrophil actin deficiency (8001052)
CL Item
Other CID (8001057)
CL Item
Wiskott Aldrich syndrome (8001131)
CL Item
Familial lymphohistiocytosis (8001132)
CL Item
Interferon g deficiency (8001133)
CL Item
X-linked lymphoproliferative (Purtilo) (8001134)
CL Item
Ataxia telangiectasia (8001135)
CL Item
Di George syndrome (8001136)
CL Item
CD40 ligand deficiency (Hyper IgM/Ig deficienc) (8001137)
CL Item
Cartilage hair hypoplasia (Dyskeratosis congen) (8001138)
CL Item
Bare lymphocyte/MHC class II/HLA-antig xp def (8001139)
CL Item
Griscelli syndrome (8001140)
CL Item
IPEX syndrome (8001141)
CL Item
Chediak-Higashi syndrome (8001151)
CL Item
Chronic granulomatous disease (8001152)
CL Item
Agranulocytosis (Kostmann) (8001153)
CL Item
Leukocyte adhesion deficiency (LAD) (8001154)
CL Item
Other primaryimmune deficiency (8001777)
CL Item
Unknown primaryimmune deficiency (8001999)
CL Item
Mucopolysaccharidoses, unspecified (8002010)
CL Item
Hurler (8002011)
CL Item
Scheie (8002012)
CL Item
Hurler/Scheie (8002013)
CL Item
Hunter (8002014)
CL Item
Sanfilippo A (8002015)
CL Item
Sanfilippo B (8002016)
CL Item
Sanfilippo C (8002017)
CL Item
Sanfilippo D (8002018)
CL Item
Morquio (IV) (8002019)
CL Item
Mucopolis V (8002021)
CL Item
Maroteaux-Lamy (8002022)
CL Item
B-glucuronidase deficiency/Type VII / Sly (8002023)
CL Item
Sphingolipidoses, unspecified (8002030)
CL Item
Metachromatic leucodystrophy (8002031)
CL Item
Multiple sulphatidosis (8002032)
CL Item
Fabry / alpha-D-galactosidase (8002033)
CL Item
GM1 ganglios (8002034)
CL Item
GM2 gangl T1 (8002035)
CL Item
GM3 gangl T2 (8002036)
CL Item
NiemPick AB (8002037)
CL Item
NiemPick CDE (8002038)
CL Item
Gaucher (8002039)
CL Item
Neuronal ceriod-lipofuscinosis (Batten disease) (8002040)
CL Item
Krabbe (8002041)
CL Item
Mucolipidose (8002050)
CL Item
Mucolipid I (8002051)
CL Item
I-cell disea (8002052)
CL Item
MucolipidIII (8002053)
CL Item
Fucosidosis (8002054)
CL Item
Mannosidosis (8002055)
CL Item
Aspartyl glucosaminuria/glucosaminidase (8002061)
CL Item
B-d-mannosid (8002062)
CL Item
N-acetyl-alpha-D-galactosaminase deficiency (8002063)
CL Item
Wolman disease/acid lipase (8002064)
CL Item
Adrenoleukodistrophy (8002070)
CL Item
Glucose storage disease (8002071)
CL Item
Lesch-Nyhan (8002072)
CL Item
Erythropoietic porphyria/Gunther`s (8002080)
CL Item
Disorders of metabolism Other (8002777)
CL Item
Disorders of metabolism unknown (8002999)
Item
Subclassification of other inherited disorder
text
CL Item
Platelet defect, unspecified (8003020)
CL Item
Glanzmann (8003021)
CL Item
Congenital amegakaryocytosis/thrombocytopaenia (8003022)
CL Item
Osteoclast defect, unspecified (8003040)
CL Item
Osteopetrosis (8003041)
CL Item
Other inherited disorders (8003077)
CL Item
Other unknown inherited disorders (8003099)
Item
Subclassification of connective tissue disease
text
CL Item
Systemic sclerosis (10001001)
CL Item
Systemic lupus erythematosus (10001002)
CL Item
Polymyositis-dermatomyositis (10001003)
CL Item
Sjogren syndrome (10001004)
CL Item
Antiphospholipid syndrome (10001005)
CL Item
Connective tissue disease Other (10001077)
CL Item
Connective tissue disease unknown (10001099)
CL Item
Wegener granulomatosis (10002001)
CL Item
Classical polyarteritis nodosa (10002002)
CL Item
Microscopic polyarteritis nodosa (10002003)
CL Item
Churg-Strauss (10002004)
CL Item
Necrotising arteritis (10002005)
CL Item
Giant cell arteritis (10002006)
CL Item
Takayasu (10002007)
CL Item
Behcets syndrome (10002008)
CL Item
Vasculitis Other (10002077)
CL Item
Vasculitis unknown (10002099)
CL Item
Rheumatoid arthritis (10003001)
CL Item
Psoriatic arthritis/psoriasis (10003002)
CL Item
Juvenile idiopathic arthritis: Systemic (Stills) (10003003)
CL Item
Juvenile idiopathic arthritis: Polyarticular (10003004)
CL Item
Juvenile idiopathic arthritis: Other (10003005)
CL Item
Arthristis other (10003077)
CL Item
Arthristis unknown (10003099)
CL Item
Myasthenia gravis (10005001)
CL Item
Other neurological (10005077)
CL Item
Unknown other neurological (10005099)
CL Item
Idiopathic thrombocytopenic purpura (ITP) (10006001)
CL Item
Idiopathic haemolytic anaemia (10006002)
CL Item
Pure red cell (acquired PRCA) (10006003)
CL Item
Pure white cell (10006004)
CL Item
Evan syndrome/combine (10006005)
CL Item
Other haematological (10006077)
CL Item
Unknown haematological (10006099)
CL Item
Crohns disease (10007001)
CL Item
Ulcerative colitis (10007002)
CL Item
Other bowel disease (10007077)
CL Item
Unknown bowel disease (10007099)