Disease #05707 (JBTS35 (Joubert syndrome, type 35 (JBTS35)), OMIM:618161)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

	Curator: Global Variome, with Curator vacancy

Official abbreviation	JBTS35
Name	Joubert syndrome, type 35 (JBTS35)
OMIM ID	618161
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ARL3
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-02-26 12:19:27 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.