Disease #05277 (PEHO (PEHO syndrome (PEHO)), OMIM:260565)

Official abbreviation PEHO
Name PEHO syndrome (PEHO)
OMIM ID 260565
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene ZNHIT3
Associated tissues -
Disease features progressive encephalopathy (HP:0002448), edema (HP:0000969), hypsarrhythmia (HP:0002521), optic atrophy (HP:0000648)
Remarks -
Date created 2017-06-02 22:02:29 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00229643 patient PubMed: Õunap 2020, Journal: Õunap 2020 2-generation family, 1 affected, unaffected heterozygous carrier parents F no Estonia - >08y - - - PEHO see paper - ZNHIT3 2 1 Sander Pajusalu
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