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Disease association ontology term - MONDO:0005328 - eye disorder

Term summary

ID
MONDO:0005328
Name
eye disorder
Ontology or CV name
Disease association
Definition
A non-neoplastic or neoplastic disorder that affects the eye. Representative examples include conjunctivitis, glaucoma, cataract, conjunctival squamous cell carcinoma, uveal melanoma, and retinoblastoma.

Parents

Annotation

Disease association

MONDO:0012099 - AICA-ribosiduria

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MONDO:0014937 - aniridia 2

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MONDO:0014720 - autosomal dominant optic atrophy plus syndrome

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MONDO:0008134 - autosomal dominant optic atrophy, classic form

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MONDO:0009815 - autosomal recessive osteopetrosis 1

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MONDO:0012676 - autosomal recessive osteopetrosis 4

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MONDO:0008858 - Behr syndrome

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MONDO:0008206 - benign paroxysmal tonic upgaze of childhood with ataxia

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MONDO:0013411 - cataract 16 multiple types

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MONDO:0011547 - cataract 31 multiple types

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MONDO:0013859 - cataract 38

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MONDO:0014565 - cataract 43

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MONDO:0014673 - cataract 44

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MONDO:0008925 - cataract 46 juvenile-onset

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MONDO:0032735 - cataract 48

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MONDO:0011413 - cataract 9 multiple types

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MONDO:0008955 - cerebrooculofacioskeletal syndrome 1

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MONDO:0012553 - cerebrooculofacioskeletal syndrome 2

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MONDO:0014696 - cerebrooculofacioskeletal syndrome 3

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MONDO:0012554 - cerebrooculofacioskeletal syndrome 4

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MONDO:0015026 - cerebroretinal microangiopathy with calcifications and cysts 2

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MONDO:0957264 - cerebroretinal microangiopathy with calcifications and cysts 3

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MONDO:0013644 - Charcot-Marie-Tooth disease axonal type 2O

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MONDO:0010557 - choroideremia

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MONDO:0009258 - classic galactosemia

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MONDO:0009352 - classic homocystinuria

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MONDO:0014372 - cone-rod dystrophy 19

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MONDO:0014669 - cone-rod dystrophy 21

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MONDO:0014872 - congenital stationary night blindness 1H

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MONDO:0020378 - early-onset posterior polar cataract

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MONDO:0016002 - Ehlers-Danlos syndrome, kyphoscoliotic type 1

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MONDO:0007376 - fleck corneal dystrophy

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MONDO:0009255 - galactokinase deficiency

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MONDO:0009257 - galactose epimerase deficiency

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MONDO:0018116 - galactosemia

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MONDO:0009737 - galactosialidosis

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MONDO:0005041 - glaucoma

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MONDO:0013802 - infantile cerebellar-retinal degeneration

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MONDO:0019118 - inherited retinal dystrophy

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MONDO:0013805 - intellectual disability, autosomal dominant 13

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MONDO:0014050 - isolated microphthalmia 8

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MONDO:0054771 - keratoconus 9

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MONDO:0100119 - Knobloch syndrome 2

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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:0008097 - linear nevus sebaceous syndrome

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MONDO:0024552 - linear skin defects with multiple congenital anomalies 1

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MONDO:0012481 - mevalonic aciduria

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MONDO:0009624 - microcephaly and chorioretinopathy 1

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MONDO:0014592 - microcephaly and chorioretinopathy 3

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

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MONDO:0014698 - microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome

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MONDO:0021129 - microphthalmia

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MONDO:0013783 - microphthalmia, isolated, with coloboma 7

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MONDO:0010671 - microphthalmia, syndromic 1

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MONDO:0975809 - microphthalmia/coloboma 13

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MONDO:0001586 - mucopolysaccharidosis type 1

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MONDO:0009661 - mucopolysaccharidosis type 6

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MONDO:0014611 - multiple mitochondrial dysfunctions syndrome 4

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MONDO:0032941 - myopia 27

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MONDO:0012154 - myopia 6

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MONDO:0009756 - Niemann-Pick disease type A

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MONDO:0010645 - oculocerebrorenal syndrome

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MONDO:0008133 - optic atrophy 3

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MONDO:0012543 - optic atrophy 5

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MONDO:0007429 - optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy

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MONDO:0009796 - ornithine aminotransferase deficiency

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MONDO:0957262 - osteopetrosis, autosomal recessive 9

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MONDO:0019200 - retinitis pigmentosa

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MONDO:0008379 - retinitis pigmentosa 10

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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:0009990 - Revesz syndrome

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MONDO:0015776 - rhizomelic chondrodysplasia punctata

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MONDO:0008972 - rhizomelic chondrodysplasia punctata type 1

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MONDO:0014743 - rhizomelic chondrodysplasia punctata type 5

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MONDO:0016369 - Rothmund-Thomson syndrome type 2

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MONDO:0010030 - Sjogren syndrome

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MONDO:0010035 - Smith-Lemli-Opitz syndrome

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

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MONDO:0010819 - Stargardt disease 3

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MONDO:0021548 - total early-onset cataract

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MONDO:0014296 - Warburg micro syndrome 4

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MONDO:0010485 - X-linked colobomatous microphthalmia-microcephaly-intellectual disability-short stature syndrome

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MONDO:0010216 - xeroderma pigmentosum group G

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