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
01712 BNHS Boucher Neuhauser syndrome 215470 AR - - PNPLA6 - -
04178 LNMS Laurence-Moon syndrome (LNMS) 245800 AR 2 2 PNPLA6 - -
04177 OMCS Oliver-McFarlane syndrome (OMCS) 275400 AR 4 4 PNPLA6 - -
03081 SPG39 paraplegia, spastic, type 39 (SPG-39) 612020 AR 1 1 PNPLA6 - -
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