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 24

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 Amaurosis24 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
26GTR
27HGMD
28HMDB
29ICD10
30ICD10 via Orphanet
31ICD9CM
32IUPHAR
33KEGG
36MedGen
38MeSH
39MESH via Orphanet
40MGI
43NCI
44NCIt
45NDF-RT
48NINDS
49Novoseek
51OMIM
52OMIM via Orphanet
56PubMed
57QIAGEN
62SNOMED-CT via Orphanet
66Tumor Gene Family of Databases
67UMLS
68UMLS via Orphanet