MCID: XLN155
MIFTS: 4

X-Linked Intellectual Disability, Sutherland-Haan Type

Categories: Fetal diseases, Neuronal diseases, Rare diseases

Aliases & Classifications for X-Linked Intellectual Disability, Sutherland-Haan Type

MalaCards integrated aliases for X-Linked Intellectual Disability, Sutherland-Haan Type:

Name: X-Linked Intellectual Disability, Sutherland-Haan Type 59

Characteristics:

Orphanet epidemiological data:

59

Classifications:



External Ids:

Orphanet 59 ORPHA93950

Summaries for X-Linked Intellectual Disability, Sutherland-Haan Type

MalaCards based summary : X-Linked Intellectual Disability, Sutherland-Haan Type An important gene associated with X-Linked Intellectual Disability, Sutherland-Haan Type is PQBP1 (Polyglutamine Binding Protein 1).

Related Diseases for X-Linked Intellectual Disability, Sutherland-Haan Type

Symptoms & Phenotypes for X-Linked Intellectual Disability, Sutherland-Haan Type

Drugs & Therapeutics for X-Linked Intellectual Disability, Sutherland-Haan Type

Search Clinical Trials , NIH Clinical Center for X-Linked Intellectual Disability, Sutherland-Haan Type

Genetic Tests for X-Linked Intellectual Disability, Sutherland-Haan Type

Anatomical Context for X-Linked Intellectual Disability, Sutherland-Haan Type

Publications for X-Linked Intellectual Disability, Sutherland-Haan Type

Variations for X-Linked Intellectual Disability, Sutherland-Haan Type

Expression for X-Linked Intellectual Disability, Sutherland-Haan Type

Search GEO for disease gene expression data for X-Linked Intellectual Disability, Sutherland-Haan Type.

Pathways for X-Linked Intellectual Disability, Sutherland-Haan Type

GO Terms for X-Linked Intellectual Disability, Sutherland-Haan Type

Sources for X-Linked Intellectual Disability, Sutherland-Haan Type

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 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 TGDB
71 Tocris
72 UMLS
73 UMLS via Orphanet
Content
Loading form....