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
07063 GDACCF global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies 617260 AD - - ZNF148 - -
06485 NEDISHM Neurodevelopmental disorder with impaired speech and hyperkinetic movements 618425 AR - - ZNF142 - -
03859 PAPA6 polydactyly, postaxial, type A6 (PAPA-6) 615226 AR 1 1 ZNF141 - autosomal recessive
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