Phenotype #0000135706

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	00170845
Associated disease	ataxia
Diagnosis/Initial	Hypotonia
Diagnosis/Definite	-
Phenotype details	Hypotonia, Global Developmental Delay, microcephaly, ataxia
Inheritance	Familial, autosomal recessive
Age/Examination	-
Age/Onset	00y01m?
Phenotype/Onset	-
Protein	-
Owner name	Inge Meijer
Database submission license	No license selected
Created by	Inge Meijer
Date created	2018-07-24 23:21:18 +02:00 (CEST)
Date last edited	N/A

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