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Disease association ontology term - MONDO:0004580 - retinal degeneration

Term summary

ID
MONDO:0004580
Name
retinal degeneration
Ontology or CV name
Disease association
Definition
Degeneration of the retina.

Parents

Annotation

Disease association

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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MONDO:0014669 - cone-rod dystrophy 21

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MONDO:0013802 - infantile cerebellar-retinal degeneration

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MONDO:0019118 - inherited retinal dystrophy

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MONDO:0018998 - Leber congenital amaurosis

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MONDO:0013454 - Leber congenital amaurosis 11

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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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MONDO:0009624 - microcephaly and chorioretinopathy 1

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

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MONDO:0009796 - ornithine aminotransferase deficiency

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MONDO:0019200 - retinitis pigmentosa

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MONDO:0008379 - retinitis pigmentosa 10

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MONDO:0981164 - retinitis pigmentosa 101

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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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MONDO:0010723 - retinitis pigmentosa 2

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MONDO:0012363 - retinitis pigmentosa 32

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MONDO:0012477 - retinitis pigmentosa 33

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MONDO:0012943 - retinitis pigmentosa 46

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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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MONDO:0014323 - retinitis pigmentosa 68

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MONDO:0014400 - retinitis pigmentosa 70

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MONDO:0015013 - retinitis pigmentosa 77

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MONDO:0044320 - retinitis pigmentosa 79

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MONDO:0032604 - retinitis pigmentosa 84

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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: