autosomal recessive intellectual developmental disorder 48

Summary
Definition
An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the SLC6A17 gene on chromosome 1p13.
Super Class
autosomal recessive intellectual developmental disorder
Disease Ontology
DOID:0081212
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
388662 SLC6A17 solute carrier family 6 member 17
Displaying 1 entry
Gene ID Gene Symbol Description Source
229706 Slc6a17 solute carrier family 6 (neurotransmitter transporter), member 17
Displaying 1 entry
Gene ID Gene Symbol Description Source
613226 Slc6a17 solute carrier family 6 member 17

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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