Phenotype #0000153671

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	00205500
Associated disease	HMN
Phenotype details	4-generation family, 6 affecteds
Diagnosis/Initial	spinal muscular atrophy
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	HMN-5A
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2012-11-05 15:40:28 +01:00 (CET)
Date last edited	N/A

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