Disease #00169 (EDS (Ehlers-Danlos syndrome), OMIM:130000)

MyGenome LOVD - This database is for training purposes only

LOVD v.3.0 Build 30 [ Current LOVD status ]
Log in

Official abbreviation	EDS
Name	Ehlers-Danlos syndrome
OMIM ID	130000
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 9 genes	ADAMTS2, COL1A1, COL1A2, COL3A1, COL5A1, COL5A2, FKBP14, PLOD1, TNXB
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-08-01 11:03:44 +02:00 (CEST)
Date last edited	N/A