Disease #01152 (JBTS20 (Joubert syndrome, type 20 (JBTS-20)), OMIM:614970)

Official abbreviation JBTS20
Name Joubert syndrome, type 20 (JBTS-20)
OMIM ID 614970
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene TMEM231
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

3 entries on 1 page. Showing entries 1 - 3.
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00063264 - - - - - - - - - - - JBTS20 - TMEM231 TMEM231 1 1 Joshi Stephen
00063266 - - - - - - - - - - - JBTS20 - TMEM231 TMEM231 1 1 Joshi Stephen
00063267 - - - - - - - - - - - JBTS20 - TMEM231 TMEM231 1 1 Joshi Stephen
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