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
04584 CPSFS1A contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A 178110 AD 10 10 MYH3 - -
05815 CPSFS1B contractures, pterygia, and spondylocarpotarsal fusion syndrome, type 1B 618469 AR 1 1 MYH3 - -
01607 DA2A arthrogryposis, distal, type 2A (DA-2A, Freeman-Sheldon syndrome) 193700 AD - - MYH3 - -
02383 DA2B1 arthrogryposis, distal, type 2B1a 601680 AD - - MYH3, TNNI2, TNNT3, TPM2 - -
06373 DA2B3 Arthrogryposis, distal, type 2B3 (Sheldon-Hall) 618436 AD - - MYH3 - -
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