All diseases

7 entries on 1 page. Showing entries 1 - 7.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00204 AD Alzheimer disease (AD) 104300 AD 697 164 A2M, ACE, APBB2, APP, BLMH, HFE, MPO, NOS3, PAXIP1, PLAU, PRNP, SORL1 - -
06652 CMT2W Charcot-Marie-Tooth disease, axonal, type 2W 616625 AD - - HACE1 - -
00256 ICH hemorrhage, intracerebral, susceptibility to (ICH) 614519 - - - ACE, COL4A1, COL4A2 - -
00255 MVCD3 microvascular complications of diabetes, susceptibility, type 3 (MVCD-3) 612624 - - - ACE - -
06119 PLDECO ?Leukodystrophy, progressive, early childhood-onset 617762 AR - - ACER3 - -
00254 RTD dysgenesis, renal tubular (RTD) 267430 AR 50 50 ACE, AGT, AGTR1, REN - -
06691 SPPRS Spastic paraplegia and psychomotor retardation with or without seizures 616756 AR - - HACE1 - -
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