All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06358 MGRISCE2 microcephaly, growth restriction, and increased sister chromatid exchange, type 2 618097 AR - - TOP3A - growth restriction, microcephaly, no malar rash, cardiomyopathy, elevated sister chromatid exchanges
06359 PEOB5 ?Progressive external ophthalmoplegia with Mi DNA deletions, autosomal recessive 5 618098 AR - - TOP3A - -
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