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Date: Tue Jan 28 2025
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Gene
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Disease Group
monogenic disease
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sensory system disease
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Genes
C18B2.4 (Cel)
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WBP2 (Hsa)
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Wbp2 (Dme)
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Wbp2 (Mmu)
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Caenorhabditis elegans
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Disease
Genes: wbp2.L (Xla)
autosomal recessive nonsyndromic deafness 107
Disease
Source:
DOID:0080262
Definition:
An autosomal recessive nonsyndromic deafness that has_material_basis_in compound heterozygous mutation in the WBP2 gene on chromosome 17q25.
Genes:
wbp2.L (Xla)
Gene (10)
Page 1 of 1
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