All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06647 HH25 Hypogonadotropic hypogonadism 25 with anosmia 618841 AD - - NDNF - -
05188 LICS lung disease, immunodeficiency, chromosome breakage syndrome (LICS) - - 5 5 NDNL2 brain;lung lung disease, immunodeficiency, chromosome instability
06265 LICS Lung disease, immunodeficiency, and chromosome breakage syndrome 617241 AR - - NDNL2 - -
00229 PWS Prader-Willi syndrome (PWS) 176270 AD 1 2 NDN, SNRPN - -
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