MCID: MSN011
MIFTS: 5

Mesangioproliferative Glomerulopathy

Categories: Rare diseases

Aliases & Classifications for Mesangioproliferative Glomerulopathy

MalaCards integrated aliases for Mesangioproliferative Glomerulopathy:

Name: Mesangioproliferative Glomerulopathy 49
Mespgn 49

Classifications:



Summaries for Mesangioproliferative Glomerulopathy

MalaCards based summary : Mesangioproliferative Glomerulopathy, is also known as mespgn. An important gene associated with Mesangioproliferative Glomerulopathy is ACE (Angiotensin I Converting Enzyme).

Related Diseases for Mesangioproliferative Glomerulopathy

Symptoms & Phenotypes for Mesangioproliferative Glomerulopathy

Drugs & Therapeutics for Mesangioproliferative Glomerulopathy

Search Clinical Trials , NIH Clinical Center for Mesangioproliferative Glomerulopathy

Genetic Tests for Mesangioproliferative Glomerulopathy

Anatomical Context for Mesangioproliferative Glomerulopathy

Publications for Mesangioproliferative Glomerulopathy

Articles related to Mesangioproliferative Glomerulopathy:

# Title Authors Year
1
Genetical, histological, and clinical characteristics of IgA-negative mesangioproliferative glomerulopathy. ( 19937361 )
2010
2
Chronic thrombopoietin overexpression induces mesangioproliferative glomerulopathy in mice. ( 17546634 )
2007

Variations for Mesangioproliferative Glomerulopathy

Expression for Mesangioproliferative Glomerulopathy

Search GEO for disease gene expression data for Mesangioproliferative Glomerulopathy.

Pathways for Mesangioproliferative Glomerulopathy

GO Terms for Mesangioproliferative Glomerulopathy

Sources for Mesangioproliferative Glomerulopathy

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
16 ExPASy
18 FMA
27 GO
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29 HGMD
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 MedGen
41 MeSH
42 MESH via Orphanet
43 MGI
45 NCI
46 NCIt
47 NDF-RT
50 NINDS
51 Novoseek
53 OMIM
54 OMIM via Orphanet
58 PubMed
60 QIAGEN
65 SNOMED-CT via HPO
66 SNOMED-CT via Orphanet
67 TGDB
68 Tocris
69 UMLS
70 UMLS via Orphanet
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