Disease #00959 (dysplasia, otodental, chromsome deletion syndrome)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Peter Thijssen

Official abbreviation	-
Name	dysplasia, otodental, chromsome deletion syndrome
OMIM ID	-
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 2 genes	FADD, FGF3
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2016-07-05 08:24:40 +02:00 (CEST)

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