Disease #00871 (dysplasia, cranioectodermal, type 2, OMIM:613610)

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	Curator: Johan T. den Dunnen

Official abbreviation	-
Name	dysplasia, cranioectodermal, type 2
OMIM ID	613610
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	WDR35
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A