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Disease association ontology term - MONDO:0019118 - inherited retinal dystrophy

Term summary

ID
MONDO:0019118
Name
inherited retinal dystrophy
Ontology or CV name
Disease association
Definition
An instance of retinal degeneration that is caused by an inherited modification of the individual's genome.

Parents

Annotation

Disease association

MONDO:0019118 - inherited retinal dystrophy

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Genes:

MONDO:0012099 - AICA-ribosiduria

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Genes:

MONDO:0010557 - choroideremia

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Genes:

MONDO:0014372 - cone-rod dystrophy 19

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Genes:

MONDO:0014669 - cone-rod dystrophy 21

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MONDO:0013802 - infantile cerebellar-retinal degeneration

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Genes:

MONDO:0018998 - Leber congenital amaurosis

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Genes:

MONDO:0013454 - Leber congenital amaurosis 11

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Genes:

MONDO:0012990 - Leber congenital amaurosis 13

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MONDO:0032794 - Leber congenital amaurosis 19

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MONDO:0012056 - Leber congenital amaurosis 9

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

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Genes:

MONDO:0009624 - microcephaly and chorioretinopathy 1

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Genes:

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

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Genes:

MONDO:0009796 - ornithine aminotransferase deficiency

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Genes:

MONDO:0019200 - retinitis pigmentosa

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Genes:

MONDO:0008379 - retinitis pigmentosa 10

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Genes:

MONDO:0010828 - retinitis pigmentosa 11

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MONDO:0010806 - retinitis pigmentosa 13

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MONDO:0011075 - retinitis pigmentosa 18

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Genes:

MONDO:0010723 - retinitis pigmentosa 2

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MONDO:0012363 - retinitis pigmentosa 32

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Genes:

MONDO:0012477 - retinitis pigmentosa 33

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MONDO:0012943 - retinitis pigmentosa 46

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Genes:

MONDO:0013468 - retinitis pigmentosa 59

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MONDO:0013516 - retinitis pigmentosa 60

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MONDO:0013611 - retinitis pigmentosa 62

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MONDO:0014256 - retinitis pigmentosa 67

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Genes:

MONDO:0014323 - retinitis pigmentosa 68

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MONDO:0014400 - retinitis pigmentosa 70

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Genes:

MONDO:0015013 - retinitis pigmentosa 77

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MONDO:0044320 - retinitis pigmentosa 79

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Genes:

MONDO:0032604 - retinitis pigmentosa 84

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Genes:

MONDO:0033563 - retinitis pigmentosa 90

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MONDO:0978291 - retinitis pigmentosa 99

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Genes:

MONDO:0009990 - Revesz syndrome

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Genes:

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

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Genes:

MONDO:0010819 - Stargardt disease 3

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Genes: