All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00139 ID intellectual disability (ID) - - 1376 1132 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 526 more - -
05652 LGMDR-23 dystrophy, muscular, limb-girdle, autosomal recessive, type 23 (LGMDR-23) 618138 - 1 1 LAMA2 - -
00360 MDC dystrophy, muscular, congenital (MDC) - - 776 776 LAMA2 - -
02717 MDC-1A dystrophy, muscular, congential, merosin deficient, type 1a (MDC-1A) 607855 - 4 0 LAMA2 - -
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