Disease #05824 (JBTS30 (Joubert syndrome, type 30 (JBTS30)), OMIM:617622)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	JBTS30
Name	Joubert syndrome, type 30 (JBTS30)
OMIM ID	617622
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ARMC9
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-08-28 15:44:56 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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