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Summary Literature (0)
MIM:260565 - PEHO SYNDROME; PEHO

Xenbase Genes: ccdc88a, znhit3

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009841 - upper rhombic lip
MONDO:0020495 - PEHO-like syndrome

Disease Ontology (DO):
DOID:0080539 - PEHO syndrome