Phenotype #0000001821

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	00002907
Associated disease	HMN5A
Phenotype details	Progressive spastic motor deficit, reactive gliosis in the spinal cord & neurogenic muscular atrophy;
Diagnosis/Initial	-
Inheritance	Unknown
Diagnosis/Definite	-
Age/Onset	-
Age/Examination	-
Age/Diagnosis	-
Protein	-
Phenotype/Onset	-
Owner name	María-Jesús Sobrido
Database submission license
Created by	Johan den Dunnen
Date created	2013-01-23 12:45:55 +01:00 (CET)
Date last edited	N/A

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