All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03396 KFS3 Klippel-Feil syndrome, type 3, autosomal dominant (KFS-3) 613702 - 1 1 GDF3 - -
03398 MCOP7 microphthalmia, isolated, type 7 (MCOP-7) 613704 AD - - GDF3 - -
03397 MCOPCB6 microphthalmia, isolated, with coloboma, type 6 (MCOPCB6) 613703 AD;DD - - GDF3, GDF6 - -
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