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MIRAGE
autosomal dominant nonsyndromic deafness 7

Summary
Synonym
  • DFNA7
  • autosomal dominant deafness 7
Definition
An autosomal dominant nonsyndromic deafness that is characterized by progressive high-tone hearing loss and has_material_basis_in variation in the chromosome region 1q21-q23.
Super Class
autosomal dominant nonsyndromic deafness
Disease Ontology
DOID:0110591
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
4009 LMX1A LIM homeobox transcription factor 1 alpha
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
Q8TE12 LIM homeobox transcription factor 1-alpha
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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

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Last updated: April 7, 2025