All diseases

6 entries on 1 page. Showing entries 1 - 6.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
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 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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