Disease #00934 (JBTS6 (Joubert syndrome, type 6 (JBTS-6)), OMIM:610688)

Official abbreviation JBTS6
Name Joubert syndrome, type 6 (JBTS-6)
OMIM ID 610688
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 TMEM67
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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00436837 20873497 Kim 2023 submitted - M ? Korea, South (Republic) Asian >28y - - - JBTS6 HP:0001252 HP:0001251 HP:0011933 HP:0000657 HP:0001249 TMEM67 TMEM67 2 1 Hyeongmin Kim
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