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Disease association ontology term - MONDO:0019588 - hearing loss, autosomal recessive

Term summary

ID
MONDO:0019588
Name
hearing loss, autosomal recessive
Ontology or CV name
Disease association
Definition
Autosomal recessive form of nonsyndromic deafness.

Parents

Annotation

Disease association

MONDO:0019588 - hearing loss, autosomal recessive

References:

Genes:

MONDO:0012091 - autosomal recessive nonsyndromic hearing loss 32

References:

Genes:

MONDO:0010933 - autosomal recessive nonsyndromic hearing loss 4

References:

Genes:

MONDO:0013471 - autosomal recessive nonsyndromic hearing loss 61

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Genes:

MONDO:0013386 - autosomal recessive nonsyndromic hearing loss 74

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Genes:

MONDO:0014237 - autosomal recessive nonsyndromic hearing loss 76

References:

Genes:

MONDO:0013489 - autosomal recessive nonsyndromic hearing loss 89

References:

Genes:

MONDO:0010986 - autosomal recessive nonsyndromic hearing loss 9

References:

Genes:

MONDO:0032740 - hearing loss, autosomal recessive 100

References:

Genes:

MONDO:0033199 - hearing loss, autosomal recessive 107

References:

Genes:

MONDO:0032639 - hearing loss, autosomal recessive 112

References:

Genes:

MONDO:0032761 - hearing loss, autosomal recessive 114

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Genes:

MONDO:0032762 - hearing loss, autosomal recessive 115

References:

Genes:

MONDO:0958277 - hearing loss, autosomal recessive 123

References:

Genes:

MONDO:0032749 - hearing loss, autosomal recessive 94

References:

Genes: