All diseases

8 entries on 1 page. Showing entries 1 - 8.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01380 FCHL3 hyperlipidemia, combined, familial 144250 AD - - LPL - -
01854 HL1 hyperlipoproteinemia, type I (lipoprotein lipase deficiency) 238600 AR 12 12 LPL - -
01865 HOPS hypophosphatasia, infantile 241500 AR 1 1 ALPL - -
05701 HPP hypophosphatasia (HPP) - AD;AR 618 617 ALPL - -
01390 HPPA hypophosphatasia, adult (odontohypophosphatasia) 146300 AD;AR 2 2 ALPL - -
01866 hypophosphatasia, childh. hypophosphatasia, childhood 241510 AR - - ALPL - -
05741 OPDM myopathy, oculopharyngodistal (OPDM) - - 60 43 GIPC1, LRP12, NOTCH2NLC, RILPL1 - -
06978 OPDM4 myopathy, oculopharyngodistal, type 4 619790 AD - - RILPL1 - -
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