MCID: SPT008

Spata7-Related Leber Congenital Amaurosis malady

Categories: Genetic diseases, Rare diseases, Eye diseases, Neuronal diseases

Aliases & Classifications for Spata7-Related Leber Congenital Amaurosis

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Aliases & Descriptions for Spata7-Related Leber Congenital Amaurosis:

Name: Spata7-Related Leber Congenital Amaurosis 24

Classifications:



Summaries for Spata7-Related Leber Congenital Amaurosis

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MalaCards based summary: Spata7-Related Leber Congenital Amaurosis An important gene associated with Spata7-Related Leber Congenital Amaurosis is SPATA7 (Spermatogenesis Associated 7).

Related Diseases for Spata7-Related Leber Congenital Amaurosis

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Symptoms & Phenotypes for Spata7-Related Leber Congenital Amaurosis

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Drugs & Therapeutics for Spata7-Related Leber Congenital Amaurosis

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Interventional clinical trials:

Search ClinicalTrials, NIH Clinical Center for Spata7-Related Leber Congenital Amaurosis

Genetic Tests for Spata7-Related Leber Congenital Amaurosis

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Genetic tests related to Spata7-Related Leber Congenital Amaurosis:

id Genetic test Affiliating Genes
1 Spata7-Related Leber Congenital Amaurosis24 SPATA7

Anatomical Context for Spata7-Related Leber Congenital Amaurosis

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Publications for Spata7-Related Leber Congenital Amaurosis

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Variations for Spata7-Related Leber Congenital Amaurosis

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Expression for genes affiliated with Spata7-Related Leber Congenital Amaurosis

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Search GEO for disease gene expression data for Spata7-Related Leber Congenital Amaurosis.

Pathways for genes affiliated with Spata7-Related Leber Congenital Amaurosis

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GO Terms for genes affiliated with Spata7-Related Leber Congenital Amaurosis

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Sources for Spata7-Related Leber Congenital Amaurosis

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2CDC
6CNVD
10DGIdb
15ExPASy
16FDA
17FMA
27GTR
28HGMD
29HMDB
30ICD10
31ICD10 via Orphanet
32ICD9CM
33IUPHAR
34KEGG
37MedGen
39MeSH
40MESH via Orphanet
41MGI
44NCI
45NCIt
46NDF-RT
49NINDS
50Novoseek
52OMIM
53OMIM via Orphanet
57PubMed
58QIAGEN
63SNOMED-CT via Orphanet
67Tumor Gene Family of Databases
68UMLS
69UMLS via Orphanet