MCID: XLN101
MIFTS: 11

X-Linked Complex Spastic Paraplegia

Categories: Neuronal diseases, Rare diseases

Aliases & Classifications for X-Linked Complex Spastic Paraplegia

MalaCards integrated aliases for X-Linked Complex Spastic Paraplegia:

Name: X-Linked Complex Spastic Paraplegia 58
X-Linked Complicated Spastic Paraplegia 58
Complicated X-Linked Hsp 58
Complicated X-Linked Spg 58
Complex X-Linked Hsp 58
Complex X-Linked Spg 58

Classifications:

Orphanet: 58  
Rare neurological diseases


External Ids:

ICD10 via Orphanet 33 G11.4
Orphanet 58 ORPHA98888

Summaries for X-Linked Complex Spastic Paraplegia

MalaCards based summary : X-Linked Complex Spastic Paraplegia, also known as x-linked complicated spastic paraplegia, is related to x-linked complicated spastic paraplegia type 1 and spastic paraplegia 16, x-linked.

Related Diseases for X-Linked Complex Spastic Paraplegia

Diseases related to X-Linked Complex Spastic Paraplegia via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 x-linked complicated spastic paraplegia type 1 12.7
2 spastic paraplegia 16, x-linked 11.7
3 paraplegia 10.4
4 masa syndrome 10.3
5 hydrocephalus 10.3
6 allan-herndon-dudley syndrome 10.1
7 mental retardation, x-linked, syndromic, claes-jensen type 10.1
8 hypotonia 10.1

Graphical network of the top 20 diseases related to X-Linked Complex Spastic Paraplegia:



Diseases related to X-Linked Complex Spastic Paraplegia

Symptoms & Phenotypes for X-Linked Complex Spastic Paraplegia

Drugs & Therapeutics for X-Linked Complex Spastic Paraplegia

Search Clinical Trials , NIH Clinical Center for X-Linked Complex Spastic Paraplegia

Genetic Tests for X-Linked Complex Spastic Paraplegia

Anatomical Context for X-Linked Complex Spastic Paraplegia

Publications for X-Linked Complex Spastic Paraplegia

Articles related to X-Linked Complex Spastic Paraplegia:

# Title Authors PMID Year
1
Novel mutations in the L1CAM gene support the complexity of L1 syndrome. 61
20447653 2010
2
Prenatal diagnosis in a family with X-linked hydrocephalus. 61
16088863 2005
3
Novel syndromic form of X-linked complicated spastic paraplegia. 61
10982473 2000
4
L1-associated diseases: clinical geneticists divide, molecular geneticists unite. 61
9300653 1997
5
A deletion of five nucleotides in the L1CAM gene in a Japanese family with X-linked hydrocephalus. 61
8786080 1996
6
Mutations in L1-CAM in two families with X linked complicated spastic paraplegia, MASA syndrome, and HSAS. 61
7562969 1995
7
Spectrum of X-linked hydrocephalus (HSAS), MASA syndrome, and complicated spastic paraplegia (SPG1): Clinical review with six additional families. 61
7645588 1995
8
X linked complicated spastic paraplegia, MASA syndrome, and X linked hydrocephalus owing to congenital stenosis of the aqueduct of Sylvius: variable expression of the same mutation at Xq28. 61
1870106 1991

Variations for X-Linked Complex Spastic Paraplegia

Expression for X-Linked Complex Spastic Paraplegia

Search GEO for disease gene expression data for X-Linked Complex Spastic Paraplegia.

Pathways for X-Linked Complex Spastic Paraplegia

GO Terms for X-Linked Complex Spastic Paraplegia

Sources for X-Linked Complex Spastic Paraplegia

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
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
43 MeSH
44 MESH via Orphanet
45 MGI
48 NCI
49 NCIt
50 NDF-RT
53 NINDS
54 Novoseek
56 OMIM
57 OMIM via Orphanet
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
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