MCID: RTN181
MIFTS: 4

Retinitis Pigmentosa 2, X-Linked

Categories: Rare diseases, Eye diseases

Aliases & Classifications for Retinitis Pigmentosa 2, X-Linked

MalaCards integrated aliases for Retinitis Pigmentosa 2, X-Linked:

Name: Retinitis Pigmentosa 2, X-Linked 53
Rp 2 53

Classifications:

MalaCards categories:
Global: Rare diseases
Anatomical: Eye diseases


Summaries for Retinitis Pigmentosa 2, X-Linked

MalaCards based summary : Retinitis Pigmentosa 2, X-Linked, also known as rp 2, is related to retinitis pigmentosa 2. An important gene associated with Retinitis Pigmentosa 2, X-Linked is RP2 (RP2, ARL3 GTPase Activating Protein).

Related Diseases for Retinitis Pigmentosa 2, X-Linked

Diseases in the Retinitis Pigmentosa, Y-Linked family:

Retinitis Pigmentosa 2, X-Linked

Diseases related to Retinitis Pigmentosa 2, X-Linked via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 retinitis pigmentosa 2 11.6

Symptoms & Phenotypes for Retinitis Pigmentosa 2, X-Linked

Drugs & Therapeutics for Retinitis Pigmentosa 2, X-Linked

Search Clinical Trials , NIH Clinical Center for Retinitis Pigmentosa 2, X-Linked

Genetic Tests for Retinitis Pigmentosa 2, X-Linked

Anatomical Context for Retinitis Pigmentosa 2, X-Linked

Publications for Retinitis Pigmentosa 2, X-Linked

Variations for Retinitis Pigmentosa 2, X-Linked

Expression for Retinitis Pigmentosa 2, X-Linked

Search GEO for disease gene expression data for Retinitis Pigmentosa 2, X-Linked.

Pathways for Retinitis Pigmentosa 2, X-Linked

GO Terms for Retinitis Pigmentosa 2, X-Linked

Sources for Retinitis Pigmentosa 2, X-Linked

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 ExPASy
19 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 LOVD
42 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
54 NINDS
55 Novoseek
57 OMIM
58 OMIM via Orphanet
62 PubMed
64 QIAGEN
69 SNOMED-CT via HPO
70 SNOMED-CT via Orphanet
71 TGDB
72 Tocris
73 UMLS
74 UMLS via Orphanet
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