Phenotype #0000210655

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Individual ID	00275973
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 19:15:30 +01:00 (CET)
Date last edited	N/A

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