All diseases

6 entries on 1 page. Showing entries 1 - 6.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03549 - deficiency, plasma fibronectin 614101 - - - FN1 - -
04255 ALS sclerosis, lateral, amyotrophic (ALS) - - 471 442 GLE1, LRP12, PFN1 - -
03729 ALS18 sclerosis, lateral, amyotrophic, type 18 (ALS18) 614808 - - - PFN1 - -
06333 BDPLT20 Bleeding disorder, platelet-type, 20 616913 AD - - SLFN14 - -
02402 GFND2 glomerulopathy, with fibronectin deposits, type 2 (GFND-2) 601894 AD - - FN1 - autosomal dominant
05367 SMDCF dysplasia, spondylometaphyseal, corner fracture type (SMDCF) 184255 AD - - FN1 - autosomal dominant
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