MCID: PLG011
MIFTS: 5

Plg-Related Hereditary Angioedema with Normal C1inh

Categories: Bone diseases, Immune diseases, Rare diseases

Aliases & Classifications for Plg-Related Hereditary Angioedema with Normal C1inh

MalaCards integrated aliases for Plg-Related Hereditary Angioedema with Normal C1inh:

Name: Plg-Related Hereditary Angioedema with Normal C1inh 59
Plg-Related Hae with Normal C1 Inhibitor 59

Classifications:



External Ids:

Orphanet 59 ORPHA537072

Summaries for Plg-Related Hereditary Angioedema with Normal C1inh

MalaCards based summary : Plg-Related Hereditary Angioedema with Normal C1inh, is also known as plg-related hae with normal c1 inhibitor. An important gene associated with Plg-Related Hereditary Angioedema with Normal C1inh is PLG (Plasminogen). Affiliated tissues include bone.

Related Diseases for Plg-Related Hereditary Angioedema with Normal C1inh

Symptoms & Phenotypes for Plg-Related Hereditary Angioedema with Normal C1inh

Drugs & Therapeutics for Plg-Related Hereditary Angioedema with Normal C1inh

Search Clinical Trials , NIH Clinical Center for Plg-Related Hereditary Angioedema with Normal C1inh

Genetic Tests for Plg-Related Hereditary Angioedema with Normal C1inh

Anatomical Context for Plg-Related Hereditary Angioedema with Normal C1inh

MalaCards organs/tissues related to Plg-Related Hereditary Angioedema with Normal C1inh:

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Bone

Publications for Plg-Related Hereditary Angioedema with Normal C1inh

Variations for Plg-Related Hereditary Angioedema with Normal C1inh

Expression for Plg-Related Hereditary Angioedema with Normal C1inh

Search GEO for disease gene expression data for Plg-Related Hereditary Angioedema with Normal C1inh.

Pathways for Plg-Related Hereditary Angioedema with Normal C1inh

GO Terms for Plg-Related Hereditary Angioedema with Normal C1inh

Sources for Plg-Related Hereditary Angioedema with Normal C1inh

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
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