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
03646 ADCL2 cutis laxa, autosomal dominant, type 2 (ADCL-2) 614434 AD 0 0 FBLN5 - -
01732 ARCL1A cutis laxa, autosomal recessive, type IA (ARCL-1A) 219100 AR 2 2 FBLN5 - -
00347 ARMD macular degeneration, age-related (ARMD) - - 29 33 ABCA4, CFH, FBLN5, HMCN1 - -
02800 HNARMD Neuropathy, hereditary, with or without age-related macular degeneration 608895 AD 0 0 FBLN5 - -
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