All diseases

11 entries on 1 page. Showing entries 1 - 11.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03072 ALS9 sclerosis, lateral, amyotrophic, type type 9 (ALS9) 611895 - - - ANG - -
04357 FHBL2 hypobetalipoproteinemia, familial, type 2 (FHBL2) 605019 AR - - ANGPTL3 - -
06944 HAE angioedema, hereditary - - 4 15 ANGPT1, HS3ST6, KNG1, MYOF, PLG, SERPING1 - -
07158 HAE5 angioedema, hereditary, type 5 619361 AD - - ANGPT1 - -
00050 hydrops fetalis hydrops fetalis - - 9 8 ANGPT2 - -
05780 LMPHM lymphatic malformation (LMPHM) - - 6 6 ANGPT2 - -
06903 LMPHM10 lymphatic malformation, type 10 619369 AD - - ANGPT2 - -
06537 MECRCN Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration 616878 AR - - TANGO2 - -
00860 NTD neural tube defects, susceptibility to (NTD) 182940 AD 101 69 FUZ, T, VANGL1, VANGL2 - -
00859 SDAM Caudal regression syndrome 600145 AD - - VANGL1 - -
04118 TGQTL plasma triglyceride level, quantitative trait locus (TGQTL) 615881 AD - - ANGPTL4 - -
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