Disease #00026 (arthrogryposis, congenital)

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Official abbreviation	-
Name	arthrogryposis, congenital
OMIM ID	-
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	GLE1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-08-03 16:49:36 +02:00 (CEST)
Date last edited	N/A