Phenotype #0000000920

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00001766
Associated disease	EDS
Inheritance	Familial
Diagnosis/Initial	-
Age/Examination	-
Diagnosis/Definite	-
Age/Onset	-
Phenotype/Onset	-
Phenotype details	ascertainment ; clinical presentation
Hearing/Loss	-
Protein	-
CK-level	-
EMG	-
Muscle/Biopsy	-
Age/Diagnosis	-
Owner name	Division of Human Genetics, Innsbruck
Database submission license
Created by	Division of Human Genetics, Innsbruck
Date created	2010-07-28 16:19:57 +02:00 (CEST)
Date last edited	N/A

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