MRX42
MCID: MNT205
MIFTS: 13

Mental Retardation, X-Linked 42 (MRX42)

Categories: Genetic diseases, Mental diseases, Neuronal diseases, Rare diseases

Aliases & Classifications for Mental Retardation, X-Linked 42

MalaCards integrated aliases for Mental Retardation, X-Linked 42:

Name: Mental Retardation, X-Linked 42 58 13 74
Mrx42 58

Classifications:



External Ids:

OMIM 58 300372
UMLS 74 C1845810

Summaries for Mental Retardation, X-Linked 42

MalaCards based summary : Mental Retardation, X-Linked 42, also known as mrx42, is related to autism x-linked 2 and cone-rod dystrophy and hearing loss 2. An important gene associated with Mental Retardation, X-Linked 42 is MRX42 (Mental Retardation, X-Linked 42).

Description from OMIM: 300372

Related Diseases for Mental Retardation, X-Linked 42

Symptoms & Phenotypes for Mental Retardation, X-Linked 42

Clinical features from OMIM:

300372

Drugs & Therapeutics for Mental Retardation, X-Linked 42

Search Clinical Trials , NIH Clinical Center for Mental Retardation, X-Linked 42

Genetic Tests for Mental Retardation, X-Linked 42

Anatomical Context for Mental Retardation, X-Linked 42

Publications for Mental Retardation, X-Linked 42

Articles related to Mental Retardation, X-Linked 42:

# Title Authors Year
1
MRX42: two linkage intervals, one in the pericentromeric region and one in Xq26, and the impact for carrier risk estimation. ( 11807862 )
2002

Variations for Mental Retardation, X-Linked 42

Expression for Mental Retardation, X-Linked 42

Search GEO for disease gene expression data for Mental Retardation, X-Linked 42.

Pathways for Mental Retardation, X-Linked 42

GO Terms for Mental Retardation, X-Linked 42

Sources for Mental Retardation, X-Linked 42

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
20 FMA
29 GO
30 GTR
31 HGMD
32 HMDB
33 HPO
34 ICD10
35 ICD10 via Orphanet
36 ICD9CM
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41 LOVD
43 MedGen
45 MeSH
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47 MGI
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52 NDF-RT
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63 PubMed
65 QIAGEN
70 SNOMED-CT via HPO
71 SNOMED-CT via Orphanet
72 TGDB
73 Tocris
74 UMLS
75 UMLS via Orphanet
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