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
06317 HPE12 Holoprosencephaly 12, with or without pancreatic agenesis 618500 AD - - CNOT1 - -
06882 VIBOS Vissers-Bodmer syndrome 619033 AD 1 1 CNOT1 - -
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