Phenotype #0000242621

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

Individual ID	00322865
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	Sofie Symoens
Database submission license	No license selected
Created by	Sofie Symoens
Date created	2011-09-27 13:13:27 +02:00 (CEST)
Date last edited	2013-05-23 13:07:43 +02:00 (CEST)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.