Phenotype #0000045731

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00059134
Associated disease	SPG11
Phenotype details	spastic paraplegia, ataxia, cognitive deficit, atrophy of the corpus callosum, motor demyelination mixed with axonal degeneration
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	29y (29 years)
Age/Diagnosis	-
Age/Onset	24y
Phenotype/Onset	spastic ataxia
Protein	-
Owner name	Mahmoud Koko
Database submission license	No license selected
Created by	Mahmoud Koko
Date created	2016-03-04 09:42:35 +01:00 (CET)
Date last edited	2016-03-18 16:27:14 +01:00 (CET)

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