All diseases

26 entries on 1 page. Showing entries 1 - 26.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01164 - adenosine triphosphate, elevated, erythrocytes 102900 - - - PKLR - -
01524 - cancer, prostate 176807 - - - AR, BRCA2, CD82, CDH1, CHEK2, HIP1, KLF6, MAD1L1, MSR1, MXI1, PTEN, ZFHX3 - -
02045 - pyruvate kinase deficiency, red cells 266200 - - - PKLR - -
03138 - prekallikrein deficiency 612423 - - - KLKB1 - -
03139 - myoclonus epilepsy with ataxia, progressive 612437 - - - PRICKLE1 - -
03381 - cancer, gastric (Neoplasm of stomach) 613659 - - - APC, CASP10, ERBB2, FGFR2, IRF1, KLF6, MUTYH, PIK3CA - -
04547 - lymphoma, Hodgkin, susceptibility to 246000 - - - KLHDC8B - -
04548 - kallikrein, decreased urinary activity of 615953 - - - KLK1 - -
01652 AI2A-1 amelogenesis imperfecta, hypomaturation type, IIA1 (AI2A-1) 204700 - - - KLK4 - -
00230 AS Angelman syndrome (AS) 105830 - - - CDKL5, MECP2, UBE3A - -
04546 CDAN-4 anemia, dyserythropoietic, congenital, type IV (CDAN-4) 613673 - - - KLF1 - -
01843 CHL lymphoma, Hodgkin, classic (CHL) 236000 - - - KLHDC8B - -
03830 CWS-4 Cowden syndrome, type 4 (CWS-4) 615107 - - - KLLN - -
00067 EIEE-2 encephalopathy, epileptic, early infantile, type 2 (EIEE-2) 300672 - - - CDKL5 - -
03454 EPM-5 epilepsy, myoclonic, progressive, type 5 (EPM-5) 613832 - - - PRICKLE2 - -
03364 HBFQTL-6 hemoglobin, fetal, quantitative trait locus 6 (HBFQTL-6) 613566 - - - KLF1 - -
04472 HFTC calcinosis, tumoral, hyperphosphatemic, familial (HFTC) 211900 - - - FGF23, GALNT3, KL - -
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 - -
01199 INLU blood group system, Lutheran inhibitor (INLU) 111150 - - - KLF1 - -
02954 MODY-7 diabetes of the young, maturity-onset, type 7 (MODY-7) 610508 - - - KLF11 - -
03901 NEM-8 myopathy, nemaline, type 8 (NEM-8) 615348 - - - KLHL40 - -
04068 NEM-9 myopathy, nemaline, type 9 (NEM-9) 615731 - - - KLHL41 - -
03668 PHA-2D pseudohypoaldosteronism type 2D (PHA-2D) 614495 - - - KLHL3 - -
02757 RP-26 retinitis pigmentosa, type 26 (RP-26) 608380 - - - CERKL - -
03215 RP-42 retinitis pigmentosa, type 42 (RP-42) 612943 - - - KLHL7 - -
03824 SPGF-11 spermatogenic failure, type 11 (SPGF-11) 615081 - - - KLHL10 - -
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