Phenotype #0000242613

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00322830
Associated disease	EDS
Inheritance	-
Diagnosis/Initial	-
Age/Examination	-
Diagnosis/Definite	-
Age/Onset	-
Phenotype/Onset	-
Phenotype details	Osteogenesis imperfecta/Ehlers-Danlos syndrome overlap,
Hearing/Loss	-
Protein	-
CK-level	-
EMG	-
Muscle/Biopsy	-
Age/Diagnosis	-
Owner name	Marina Colombi, Marco Ritelli
Database submission license	No license selected
Created by	Marina Colombi, Marco Ritelli
Date created	2019-09-05 10:36:27 +02:00 (CEST)
Date last edited	2019-09-11 14:08:08 +02:00 (CEST)

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