Disease #00002 (JBTS-1 (Joubert syndrome, type 1 (JBTS-1)), OMIM:213300)

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	Curator: Johan T. den Dunnen

Official abbreviation	JBTS-1
Name	Joubert syndrome, type 1 (JBTS-1)
OMIM ID	213300
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 5 genes	AHI1, CEP290, INPP5E, TCTN1, TMEM67
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-05-17 22:47:36 +02:00 (CEST)
Date last edited	N/A