MCID: CRB082

Crb1-Related Leber Congenital Amaurosis malady

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

Aliases & Classifications for Crb1-Related Leber Congenital Amaurosis

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Aliases & Descriptions for Crb1-Related Leber Congenital Amaurosis:

Name: Crb1-Related Leber Congenital Amaurosis 23

Classifications:



Summaries for Crb1-Related Leber Congenital Amaurosis

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MalaCards based summary: Crb1-Related Leber Congenital Amaurosis An important gene associated with Crb1-Related Leber Congenital Amaurosis is CRB1 (Crumbs 1, Cell Polarity Complex Component).

Related Diseases for Crb1-Related Leber Congenital Amaurosis

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Symptoms for Crb1-Related Leber Congenital Amaurosis

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Drugs & Therapeutics for Crb1-Related Leber Congenital Amaurosis

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Interventional clinical trials:

Search ClinicalTrials, NIH Clinical Center for Crb1-Related Leber Congenital Amaurosis

Genetic Tests for Crb1-Related Leber Congenital Amaurosis

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Genetic tests related to Crb1-Related Leber Congenital Amaurosis:

id Genetic test Affiliating Genes
1 Crb1-Related Leber Congenital Amaurosis23 CRB1

Anatomical Context for Crb1-Related Leber Congenital Amaurosis

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Animal Models for Crb1-Related Leber Congenital Amaurosis or affiliated genes

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Publications for Crb1-Related Leber Congenital Amaurosis

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Variations for Crb1-Related Leber Congenital Amaurosis

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Expression for genes affiliated with Crb1-Related Leber Congenital Amaurosis

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Search GEO for disease gene expression data for Crb1-Related Leber Congenital Amaurosis.

Pathways for genes affiliated with Crb1-Related Leber Congenital Amaurosis

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GO Terms for genes affiliated with Crb1-Related Leber Congenital Amaurosis

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Sources for Crb1-Related Leber Congenital Amaurosis

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2CDC
6CNVD
10DGIdb
15ExPASy
16FDA
17FMA
25GTR
26HGMD
27HMDB
28ICD10
29ICD10 via Orphanet
30ICD9CM
31IUPHAR
32KEGG
35MedGen
37MeSH
38MESH via Orphanet
39MGI
42NCI
43NCIt
44NDF-RT
47NINDS
48Novoseek
50OMIM
51OMIM via Orphanet
55PubMed
56QIAGEN
61SNOMED-CT via Orphanet
65Tumor Gene Family of Databases
66UMLS
67UMLS via Orphanet