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Standards Ontologies Notations
autosomal recessive nonsyndromic deafness 108

Summary
Definition
An autosomal recessive nonsyndromic deafness that has_material_basis_in homozygous mutation in the ROR1 gene on chromosome 1p31.
Super Class
autosomal recessive nonsyndromic deafness
Disease Ontology
DOID:0080263
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
4919 ROR1 receptor tyrosine kinase like orphan receptor 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
26563 Ror1 receptor tyrosine kinase-like orphan receptor 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
34367 Ror Ror
Displaying 1 entry
Gene ID Gene Symbol Description Source
174473 cam-1 Tyrosine-protein kinase receptor cam-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