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Disease association ontology term - MONDO:0024417 - perceptual disorders

Term summary

ID
MONDO:0024417
Name
perceptual disorders
Ontology or CV name
Disease association
Definition
Cognitive disorders characterized by an impaired ability to perceive the nature of objects or concepts through use of the sense organs. These include spatial neglect syndromes, where an individual does not attend to visual, auditory, or sensory stimuli presented from one side of the body.

Parents

Annotation

Disease association

MONDO:0012099 - AICA-ribosiduria

References:

Genes:

MONDO:0012196 - autosomal dominant auditory neuropathy 1

References:

Genes:

MONDO:0007424 - autosomal dominant nonsyndromic hearing loss 1

References:

Genes:

MONDO:0011350 - autosomal dominant nonsyndromic hearing loss 17

References:

Genes:

MONDO:0011480 - autosomal dominant nonsyndromic hearing loss 20

References:

Genes:

MONDO:0011568 - autosomal dominant nonsyndromic hearing loss 25

References:

Genes:

MONDO:0014603 - autosomal dominant nonsyndromic hearing loss 40

References:

Genes:

MONDO:0010915 - autosomal dominant nonsyndromic hearing loss 4A

References:

Genes:

MONDO:0014594 - autosomal dominant nonsyndromic hearing loss 67

References:

Genes:

MONDO:0014853 - autosomal dominant nonsyndromic hearing loss 70

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

References:

Genes:

MONDO:0013386 - autosomal recessive nonsyndromic hearing loss 74

References:

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:0010557 - choroideremia

References:

Genes:

MONDO:0014372 - cone-rod dystrophy 19

References:

Genes:

MONDO:0014669 - cone-rod dystrophy 21

References:

Genes:

MONDO:0014872 - congenital stationary night blindness 1H

References:

Genes:

MONDO:0010799 - deafness, aminoglycoside-induced

References:

Genes:

MONDO:0027048 - deafness, Y-linked 2

References:

Genes:

MONDO:0033258 - hearing loss, autosomal dominant 71

References:

Genes:

MONDO:0032911 - hearing loss, autosomal dominant 75

References:

Genes:

MONDO:0032917 - hearing loss, autosomal dominant 76

References:

Genes:

MONDO:0030058 - hearing loss, autosomal dominant 77

References:

Genes:

MONDO:0033668 - hearing loss, autosomal dominant 79

References:

Genes:

MONDO:0030719 - hearing loss, autosomal dominant 82

References:

Genes:

MONDO:0859524 - hearing loss, autosomal dominant 86

References:

Genes:

MONDO:0859525 - hearing loss, autosomal dominant 87

References:

Genes:

MONDO:0019588 - hearing loss, autosomal recessive

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

References:

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:

MONDO:0010577 - hearing loss, X-linked 1

References:

Genes:

MONDO:0013802 - infantile cerebellar-retinal degeneration

References:

Genes:

MONDO:0019118 - inherited retinal dystrophy

References:

Genes:

MONDO:0009479 - Johanson-Blizzard syndrome

References:

Genes:

MONDO:0018998 - Leber congenital amaurosis

References:

Genes:

MONDO:0013454 - Leber congenital amaurosis 11

References:

Genes:

MONDO:0012990 - Leber congenital amaurosis 13

References:

Genes:

MONDO:0032794 - Leber congenital amaurosis 19

References:

Genes:

MONDO:0012056 - Leber congenital amaurosis 9

References:

Genes:

MONDO:0060650 - Leber congenital amaurosis with early-onset deafness

References:

Genes:

MONDO:0009624 - microcephaly and chorioretinopathy 1

References:

Genes:

MONDO:0007918 - microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability

References:

Genes:

MONDO:0019497 - nonsyndromic genetic hearing loss

References:

Genes:

MONDO:0009796 - ornithine aminotransferase deficiency

References:

Genes:

MONDO:0019200 - retinitis pigmentosa

References:

Genes:

MONDO:0008379 - retinitis pigmentosa 10

References:

Genes:

MONDO:0981164 - retinitis pigmentosa 101

References:

Genes:

MONDO:0010828 - retinitis pigmentosa 11

References:

Genes:

MONDO:0010806 - retinitis pigmentosa 13

References:

Genes:

MONDO:0011075 - retinitis pigmentosa 18

References:

Genes:

MONDO:0010723 - retinitis pigmentosa 2

References:

Genes:

MONDO:0012363 - retinitis pigmentosa 32

References:

Genes:

MONDO:0012477 - retinitis pigmentosa 33

References:

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MONDO:0012943 - retinitis pigmentosa 46

References:

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MONDO:0013468 - retinitis pigmentosa 59

References:

Genes:

MONDO:0013516 - retinitis pigmentosa 60

References:

Genes:

MONDO:0013611 - retinitis pigmentosa 62

References:

Genes:

MONDO:0014256 - retinitis pigmentosa 67

References:

Genes:

MONDO:0014323 - retinitis pigmentosa 68

References:

Genes:

MONDO:0014400 - retinitis pigmentosa 70

References:

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MONDO:0015013 - retinitis pigmentosa 77

References:

Genes:

MONDO:0044320 - retinitis pigmentosa 79

References:

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MONDO:0032604 - retinitis pigmentosa 84

References:

Genes:

MONDO:0033563 - retinitis pigmentosa 90

References:

Genes:

MONDO:0978291 - retinitis pigmentosa 99

References:

Genes:

MONDO:0009990 - Revesz syndrome

References:

Genes:

MONDO:0031007 - spondyloepiphyseal dysplasia, sensorineural hearing loss, impaired intellectual development, and leber congenital amaurosis

References:

Genes:

MONDO:0010819 - Stargardt disease 3

References:

Genes:

MONDO:0010378 - X-linked hereditary sensory and autonomic neuropathy with hearing loss

References:

Genes: