Phenotype #0000002886

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00004117
Associated disease	ID
Diagnosis/Initial	-
Diagnosis/Definite	-
Inheritance	Familial, X-linked recessive
Phenotype details	agenesis of corpus callosum, aplasia/hypoplasia of the cerebellum, microcephaly, ichthyosis
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Pamela Magini
Database submission license	No license selected
Created by	Pamela Magini
Date created	2013-12-16 11:16:35 +01:00 (CET)
Date last edited	2014-02-02 21:22:22 +01:00 (CET)

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