|
|
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CEP290
|
|
21
disease terms (MeSH) has been reported with CEP290 gene.
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[Click  to re-sort the table]
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Meta-analysis Publications
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Leber Congenital Amaurosis
|
8
|
0
|
|
Retinitis Pigmentosa
|
6
|
0
|
|
Kidney Diseases, Cystic
|
4
|
0
|
|
Retinal Diseases
|
3
|
0
|
|
Retinal Dystrophies
|
3
|
0
|
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Blindness
|
3
|
0
|
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Abnormalities, Multiple
|
2
|
0
|
|
Retinal Degeneration
|
2
|
0
|
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Mental Retardation
|
1
|
0
|
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Obesity, Morbid
|
1
|
0
|
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Optic Atrophies, Hereditary
|
1
|
0
|
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Optic Atrophy, Hereditary, Leber
|
1
|
0
|
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Heart Septal Defects
|
1
|
0
|
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Bardet-Biedl Syndrome
|
1
|
0
|
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Cerebellar Ataxia
|
1
|
0
|
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Cone-Rod Dystrophies
|
1
|
0
|
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Down Syndrome
|
1
|
0
|
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Genetic Diseases, Inborn
|
1
|
0
|
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Genetic Diseases, X-Linked
|
1
|
0
|
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Syndrome
|
1
|
0
|
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Vision Disorders
|
1
|
0
|
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Note: The number of publications displayed in this table will differ from the number displayed in the HuGE Literature Finder as the number
in Genopedia reflects only the indexed disease term without children terms, but the number in the HuGE Literature Finder
reflects all text searches of the disease term including the indexed term and corresponding children terms.
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