Phenotype #0000138573

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00173709
Associated disease	SMAX2
Phenotype details	-
Diagnosis/Initial	X-linked congenital spinal muscular atrophy
Inheritance	Familial, X-linked recessive
Diagnosis/Definite	SMAX-2
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	?
Protein	-
Owner name	Alfons Meindl
Database submission license	No license selected
Created by	Alfons Meindl
Date created	2015-01-29 14:01:10 +01:00 (CET)
Date last edited	2018-07-27 15:13:14 +02:00 (CEST)

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