Disease #04039 (JBTS21 (Joubert syndrome, type 21 (JBTS-21)), OMIM:615636)

Official abbreviation JBTS21
Name Joubert syndrome, type 21 (JBTS-21)
OMIM ID 615636
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene CSPP1
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)


Individuals

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00080861 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - JBTS21 Joubert syndrome 21 (OMIM:615636) CSPP1 CSPP1 1 1 Daniel Trujillano
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