Search results for: PTPN11

Disease (25)

Disease Description Nervous effect
D00000018 Gastric cancer N
D00000028 Lung cancer N
D00000040 Rhabdomyosarcoma N
D00000042 Breast cancer N
D00000066 Neuroblastoma Y
D00000089 Childhood acute lymphoblastic leukaemia N
D00000092 Acute myelogenous leukaemia N
D00000093 Acute myeloid leukaemia N
D00000096 Chronic myelomonocytic leukaemia N
D00000099 Juvenile myelomonocytic leukaemia N
D00000102 Paediatric acute myeloid leukaemia N
D00000117 Myelodysplastic syndrome N
D00000119 Myeloproliferative disease N
D00000233 Pulmonary valve stenosis N
D00000235 Hypertrophic cardiomyopathy N
D00000241 Cherubism N
D00000244 Gastric atrophy N
D00000278 Hydrops fetalis N
D00000285 Atrioventricular septal defect N
D00000286 Coarctation of the aorta N
D00000304 Leopard syndrome N
D00000305 Noonan syndrome N
D00000306 Noonan syndrome with growth hormone resistance N
D00000307 Noonan-like/multiple giant cell lesion syndrome N
D00000313 Aortic valvar stenosis N

Gene (2)

Gene Symbol Species Description
G00000204 Ptpn11 Mus musculus protein tyrosine phosphatase, non-receptor type 11
G00001453 PTPN11 Homo sapiens protein tyrosine phosphatase, non-receptor type 11
© G2C 2014. The Genes to Cognition Programme received funding from The Wellcome Trust and the EU FP7 Framework Programmes:
EUROSPIN (FP7-HEALTH-241498), SynSys (FP7-HEALTH-242167) and GENCODYS (FP7-HEALTH-241995).

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