Joubert syndrome 24

Summary
Synonym
  • JBTS24
Definition
A Joubert syndrome characterized by delayed psychomotor development and molar tooth sign on brain MRI that has_material_basis_in homozygous mutation in the TCTN2 gene on chromosome 12q24.
Super Class
Joubert syndrome
External Links
Disease Ontology
DOID:0110993
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
79867 TCTN2 tectonic family member 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
67978 Tctn2 tectonic family member 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
689779 Tctn2 tectonic family member 2
The Human Phenotype Ontology
Displaying entries 31 - 37 of 37 in total
HPO ID HPO Term
HP:0000426 Prominent nasal bridge
HP:0001337 Tremor
HP:0002553 Highly arched eyebrow
HP:0001161 Hand polydactyly
HP:0008872 Feeding difficulties in infancy
HP:0007370 Aplasia/Hypoplasia of the corpus callosum
HP:0030680 Abnormal cardiovascular system morphology
Displaying 1 entry
Gene ID Gene Symbol Description
56623 INPP5E inositol polyphosphate-5-phosphatase E

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024