All diseases

5 entries on 1 page. Showing entries 1 - 5.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02858 DFNB-23 deafness, autosomal recessive, type 23 (DFNB-23) 609533 - - - PCDH15 - -
00139 ID intellectual disability (ID) - - - - AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 515 more - -
01110 MRD-3 mental retardation, autosomal dominant, type 3 (MRD-3) 612580 - - - CDH15 - -
02337 USH-1D Usher syndrome, type 1D (USH-1D) 601067 - - - CDH23, PCDH15 - -
02413 USH-1F Usher syndrome, type 1F (USH-1F) 602083 - - - PCDH15 - -
Legend   How to query