Disease #00080 (JBTS7 (Joubert syndrome, type 7 (JBTS-7)), OMIM:611560)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	JBTS7
Name	Joubert syndrome, type 7 (JBTS-7)
OMIM ID	611560
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	RPGRIP1L
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-11-09 15:18:18 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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