All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05277 PEHO PEHO syndrome (PEHO) 260565 AR 1 1 ZNHIT3 - progressive encephalopathy (HP:0002448), edema (HP:0000969), hypsarrhythmia (HP:0002521), optic atrophy (HP:0000648)
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