Disease #06166 (JBTS24 (Joubert syndrome 24), OMIM:616654)

Official abbreviation JBTS24
Name Joubert syndrome 24
OMIM ID 616654
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 TCTN2
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

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00430484 - - - M no Japan - - - - - JBTS24 Developmental delay, dysmorphic facial features and polydactyly, retinal dystrophy, exotropia, abnormal pattern of respiration, and periventricular heterotopia TCTN2 TCTN2 2 1 Takuya Hiraide
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