Global Variome shared LOVD

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Phenotype #0000174479 Individual ID 00234052 Associated disease PCH6 Phenotype details severe developmental delay, seizures, microcephaly Diagnosis/Initial PEHO syndrome Inheritance Familial, autosomal recessive Diagnosis/Definite PCH6 Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Carolina Courage Database submission license No license selected Created by Carolina Courage Date created 2019-05-06 09:41:21 +02:00 (CEST) Date last edited 2019-05-06 12:11:09 +02:00 (CEST)

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