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Disease association ontology term - MONDO:0019587 - autosomal dominant nonsyndromic hearing loss

Term summary

ID
MONDO:0019587
Name
autosomal dominant nonsyndromic hearing loss
Ontology or CV name
Disease association
Definition
Autosomal dominant form of nonsyndromic deafness.

Parents

Annotation

Disease association

MONDO:0012196 - autosomal dominant auditory neuropathy 1

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Genes:

MONDO:0007424 - autosomal dominant nonsyndromic hearing loss 1

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Genes:

MONDO:0011350 - autosomal dominant nonsyndromic hearing loss 17

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MONDO:0011480 - autosomal dominant nonsyndromic hearing loss 20

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MONDO:0011568 - autosomal dominant nonsyndromic hearing loss 25

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MONDO:0014603 - autosomal dominant nonsyndromic hearing loss 40

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MONDO:0010915 - autosomal dominant nonsyndromic hearing loss 4A

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MONDO:0014594 - autosomal dominant nonsyndromic hearing loss 67

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MONDO:0014853 - autosomal dominant nonsyndromic hearing loss 70

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MONDO:0033258 - hearing loss, autosomal dominant 71

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MONDO:0032911 - hearing loss, autosomal dominant 75

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MONDO:0032917 - hearing loss, autosomal dominant 76

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MONDO:0030058 - hearing loss, autosomal dominant 77

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MONDO:0033668 - hearing loss, autosomal dominant 79

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MONDO:0030719 - hearing loss, autosomal dominant 82

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MONDO:0859524 - hearing loss, autosomal dominant 86

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MONDO:0859525 - hearing loss, autosomal dominant 87

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