All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01654 ALS2 sclerosis, lateral, amyotrophic, type type 2 (ALS2) 205100 AR - - ALS2 - -
02640 IAHSP paralysis, spastic, hereditary, ascending, infantile-onset (IAHSP) 607225 AR 2 2 ALS2 - -
02760 MCI1 myocardial infarction, susceptibility to, type 1 (MCI-1) 608446 - 41 2 ESR1, F13A1, F7, GCLC, GCLM, ITGB3, LGALS2, LTA, MIAT, OLR1, PSMA6, TNFSF4 - -
02581 PLSJ sclerosis, lateral, juvenile primary (PLSJ) 606353 AR - - ALS2 - -
06913 SPGF68 spermatogenic failure, type 68 619805 AR - - ALS2CR11 - -
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