Disease #03548 (CED3 (dysplasia, cranioectodermal, type 3 (CED3)), OMIM:614099)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CED3
Name	dysplasia, cranioectodermal, type 3 (CED3)
OMIM ID	614099
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	IFT43
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2020-04-25 16:09:24 +02:00 (CEST)

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