All diseases

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06029 MCPH20 Microcephaly 20, primary, autosomal recessive 617914 AR - - KIF14 - -
04545 MKS12 Meckel syndrome?, type 12 (MKS-12) 616258 AR 5 5 KIF14 - -
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.