Disease #04261 (SEDT (dysplasia, spondyloepiphyseal, tarda (SEDT)))

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	Curator: Johan T. den Dunnen

Official abbreviation	SEDT
Name	dysplasia, spondyloepiphyseal, tarda (SEDT)
OMIM ID	-
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	COL2A1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-05-08 12:27:03 +02:00 (CEST)
Date last edited	N/A