Disease #00582 (JBTS8 (Joubert syndrome, type 8 (JBTS-8)), OMIM:612291)

Official abbreviation JBTS8
Name Joubert syndrome, type 8 (JBTS-8)
OMIM ID 612291
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene ARL13B
Associated tissues -
Disease features -
Remarks -