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

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.1.0

Last updated: December 9, 2024