Disease #05634 (JBTS33 (Joubert syndrome, type 33 (JBTS-33)), OMIM:617767)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	JBTS33
Name	Joubert syndrome, type 33 (JBTS-33)
OMIM ID	617767
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PIBF1
Associated tissues	-
Disease features	autosomal recessive
Remarks	-
Date created	2019-07-28 13:15:45 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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