PSNP3
MCID: SPR048
MIFTS: 10

Supranuclear Palsy, Progressive, 3 (PSNP3)

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

Aliases & Classifications for Supranuclear Palsy, Progressive, 3

MalaCards integrated aliases for Supranuclear Palsy, Progressive, 3:

Name: Supranuclear Palsy, Progressive, 3 57 13 70
Psnp3 57

Classifications:



External Ids:

OMIM® 57 610898
UMLS 70 C1970476

Summaries for Supranuclear Palsy, Progressive, 3

MalaCards based summary : Supranuclear Palsy, Progressive, 3, is also known as psnp3. An important gene associated with Supranuclear Palsy, Progressive, 3 is PSNP3 (Supranuclear Palsy, Progressive, 3). Affiliated tissues include eye.

More information from OMIM: 610898

Related Diseases for Supranuclear Palsy, Progressive, 3

Diseases in the Supranuclear Palsy, Progressive, 1 family:

Supranuclear Palsy, Progressive, 2 Supranuclear Palsy, Progressive, 3

Symptoms & Phenotypes for Supranuclear Palsy, Progressive, 3

Clinical features from OMIM®:

610898 (Updated 20-May-2021)

Drugs & Therapeutics for Supranuclear Palsy, Progressive, 3

Search Clinical Trials , NIH Clinical Center for Supranuclear Palsy, Progressive, 3

Genetic Tests for Supranuclear Palsy, Progressive, 3

Anatomical Context for Supranuclear Palsy, Progressive, 3

MalaCards organs/tissues related to Supranuclear Palsy, Progressive, 3:

40
Eye

Publications for Supranuclear Palsy, Progressive, 3

Articles related to Supranuclear Palsy, Progressive, 3:

(showing 1, show less)
# Title Authors PMID Year
1
Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms. 57
17357082 2007

Variations for Supranuclear Palsy, Progressive, 3

Expression for Supranuclear Palsy, Progressive, 3

Search GEO for disease gene expression data for Supranuclear Palsy, Progressive, 3.

Pathways for Supranuclear Palsy, Progressive, 3

GO Terms for Supranuclear Palsy, Progressive, 3

Sources for Supranuclear Palsy, Progressive, 3

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
20 GARD
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
53 NINDS
54 Novoseek
56 OMIM via Orphanet
57 OMIM® (Updated 20-May-2021)
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 Tocris
70 UMLS
71 UMLS via Orphanet
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