Disease #00082 (JBTS-9 (Joubert syndrome, type 9 (JBTS-9)), OMIM:612285)

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	Curator: Johan T. den Dunnen

Official abbreviation	JBTS-9
Name	Joubert syndrome, type 9 (JBTS-9)
OMIM ID	612285
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CC2D2A
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-11-09 15:25:03 +01:00 (CET)
Date last edited	N/A