Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000210662 Individual ID 00275980 Associated disease PCH Phenotype details - Diagnosis/Initial pontocerebellar hypoplasia Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Onset - Phenotype/Onset - Protein - Owner name Enza Maria Valente Database submission license No license selected Created by Johan den Dunnen Date created 2020-01-21 19:37:53 +01:00 (CET) Date last edited N/A

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