Disease #01056 (JBTS10 (Joubert syndrome, type 10 (JBTS-10)), OMIM:300804)

Official abbreviation JBTS10
Name Joubert syndrome, type 10 (JBTS-10)
OMIM ID 300804
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene OFD1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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