All diseases

15 entries on 1 page. Showing entries 1 - 15.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00423 - cancer, endometrial 608089 - - - CDH1, MLH3, MSH3, MSH6, PTEN - -
00683 - cancer, breast, familial 114480 - - - AKT1, ATM, BARD1, BRCA1, BRCA2, BRIP1, CASP8, CDH1, CHEK2, ESR1, HMMR, KRAS, NQO2, PALB2, PHB, PIK3CA, PPM1D, RAD51, RAD54L, RB1CC1, 4 more - -
01524 - cancer, prostate 176807 - - - AR, BRCA2, CD82, CDH1, CHEK2, HIP1, KLF6, MAD1L1, MSR1, MXI1, PTEN, ZFHX3 - -
00424 cancer, ovarian cancer, ovarian 167000 - - - AKT1, CDH1, CTNNB1, OPCML, PARK2, PIK3CA - -
04254 CLP cleft lip, cleft palate (CLP) - - - - CDH1 - -
02858 DFNB-23 deafness, autosomal recessive, type 23 (DFNB-23) 609533 - - - PCDH15 - -
04252 DGC cancer, gastric, diffuse (DGC) - - - - CDH1 - -
02142 EIEE-9 encephalopathy, epileptic, early infantile, type 9 (EIEE-9) 300088 - - - PCDH19 - -
04251 EODGC cancer, gastric, diffuse, early onset (EODGC) - - - - CDH1 - -
00334 HDGC cancer, gastric, hereditary diffuse (HDGC) 137215 - - - CDH1, IL1B, IL1RN, KRAS, MUTYH - -
00139 ID intellectual disability (ID) - - - - AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 515 more - -
04253 LBC cancer, breast, lobular (LBC) - - - - CDH1 - -
01110 MRD-3 mental retardation, autosomal dominant, type 3 (MRD-3) 612580 - - - CDH15 - -
02337 USH-1D Usher syndrome, type 1D (USH-1D) 601067 - - - CDH23, PCDH15 - -
02413 USH-1F Usher syndrome, type 1F (USH-1F) 602083 - - - PCDH15 - -
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