All diseases

11 entries on 1 page. Showing entries 1 - 11.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00423 - cancer, endometrial 608089 AD;SMu 225 191 CDH1, MLH3, MSH3, MSH6, PTEN - -
02540 - macrocephaly/autism syndrome 605309 AD 1 0 PTEN - -
01420 BRRS Bannayan-Riley-Ruvalcaba syndrome (BRRS) 153480 - 5 5 PTEN - -
01524 cancer, prostate cancer, prostate 176807 AD;SMu 202 198 AR, BRCA2, CD82, CDH1, CHEK2, HIP1, KLF6, MAD1L1, MSR1, MXI1, PTEN, ZFHX3 - -
01431 CMM1 melanoma, cutaneous, malignant, susceptibility to, type 1 (CMM-1) 155600 - 0 0 PTEN - -
01445 CWS1 Cowden syndrome, type 1 (CWS1) 158350 AD 440 19 PTEN - -
03233 GLM2 glioma, susceptibility, type 2 (GLM-2) 613028 - 0 0 PTEN - -
02107 HNSCC carcinoma, squamous cell, head and neck (HNSCC) 275355 AR 5 5 ING1, PTEN, TNFRSF10B - -
02638 meningioma meningioma, familial, susceptibility to 607174 AD 65 65 MN1, NF2, PDGFB, PTEN, SMARCE1, SUFU - -
00554 NMTC2 cancer, thyroid, nonmedullary, type 2 (NMTC-2, follicular) 188470 AD;SMu 0 0 HRAS, MINPP1, NRAS, PTEN, SRGAP1 - -
04632 VATERLH VATERL association with hydrocephalus (VACTERL-H) 276950 - 0 0 PTEN - -
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