MCID: SPT008
MIFTS: 7

Spata7-Related Leber Congenital Amaurosis malady

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

Aliases & Classifications for Spata7-Related Leber Congenital Amaurosis

Aliases & Descriptions for Spata7-Related Leber Congenital Amaurosis:

Name: Spata7-Related Leber Congenital Amaurosis 24

Classifications:



Summaries for Spata7-Related Leber Congenital Amaurosis

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

Symptoms & Phenotypes for Spata7-Related Leber Congenital Amaurosis

Drugs & Therapeutics for Spata7-Related Leber Congenital Amaurosis

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

Genetic Tests for Spata7-Related Leber Congenital Amaurosis

Genetic tests related to Spata7-Related Leber Congenital Amaurosis:

id Genetic test Affiliating Genes
1 Spata7-Related Leber Congenital Amaurosis 24 SPATA7

Anatomical Context for Spata7-Related Leber Congenital Amaurosis

Publications for Spata7-Related Leber Congenital Amaurosis

Variations for Spata7-Related Leber Congenital Amaurosis

Expression for Spata7-Related Leber Congenital Amaurosis

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

Pathways for Spata7-Related Leber Congenital Amaurosis

GO Terms for Spata7-Related Leber Congenital Amaurosis

Sources for Spata7-Related Leber Congenital Amaurosis

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
16 ExPASy
18 FMA
28 GO
29 GTR
30 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
36 IUPHAR
37 KEGG
38 LifeMap
40 MedGen
42 MeSH
43 MESH via Orphanet
44 MGI
46 NCI
47 NCIt
48 NDF-RT
51 NINDS
52 Novoseek
54 OMIM
55 OMIM via Orphanet
59 PubMed
60 QIAGEN
65 SNOMED-CT via Orphanet
67 TGDB
68 Tocris
69 UMLS
70 UMLS via Orphanet
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