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Standards Ontologies Notations
autosomal dominant nonsyndromic deafness 72

Summary
Definition
An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the SLC44A4 gene on chromosome 6p21.
Super Class
autosomal dominant nonsyndromic deafness
Disease Ontology
DOID:0080268
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
80736 SLC44A4 solute carrier family 44 member 4
Displaying 1 entry
Gene ID Gene Symbol Description Source
70129 Slc44a4 solute carrier family 44, member 4
Displaying 1 entry
Gene ID Gene Symbol Description Source
294255 Slc44a4 solute carrier family 44, member 4
Displaying 1 entry
Gene ID Gene Symbol Description Source
43440 Ctl2 Choline transporter-like 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
393385 slc44a4 solute carrier family 44 member 4
Displaying 1 entry
Gene ID Gene Symbol Description Source Organism
444429 slc44a4.L solute carrier family 44 member 4 L homeolog Xenopus laevis (African clawed frog)
Displaying 1 entry
Gene ID Gene Symbol Description Source
180809 chtl-1 Choline transporter-like protein 1
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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