autosomal recessive intellectual developmental disorder 14

Summary
Definition
An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the TECR gene on chromosome 19p13.
Super Class
autosomal recessive intellectual developmental disorder
Disease Ontology
DOID:0081188
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
9524 TECR trans-2,3-enoyl-CoA reductase
Displaying 1 entry
Gene ID Gene Symbol Description Source
106529 Tecr trans-2,3-enoyl-CoA reductase
Displaying 1 entry
Gene ID Gene Symbol Description Source
191576 Tecr trans-2,3-enoyl-CoA reductase
The Human Phenotype Ontology
Displaying all 6 entries
HPO ID HPO Term
HP:0001249 Intellectual disability
HP:0000189 Narrow palate
HP:0003593 Infantile onset
HP:0000007 Autosomal recessive inheritance
HP:0002080 Intention tremor
HP:0000750 Delayed speech and language development
Displaying 1 entry
Gene ID Gene Symbol Description
9524 TECR trans-2,3-enoyl-CoA reductase

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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: December 9, 2024