MCID: RRH022
MIFTS: 7

Rare Hereditary Thrombophilia

Categories: Blood diseases, Bone diseases, Genetic diseases, Immune diseases, Rare diseases

Aliases & Classifications for Rare Hereditary Thrombophilia

MalaCards integrated aliases for Rare Hereditary Thrombophilia:

Name: Rare Hereditary Thrombophilia 58

Classifications:

Orphanet: 58  
Rare systemic and rhumatological diseases
Rare bone diseases
Rare haematological diseases


External Ids:

ICD10 via Orphanet 33 D68.5
UMLS via Orphanet 72 C2584620
Orphanet 58 ORPHA217454

Summaries for Rare Hereditary Thrombophilia

MalaCards based summary : Rare Hereditary Thrombophilia Affiliated tissues include bone.

Related Diseases for Rare Hereditary Thrombophilia

Symptoms & Phenotypes for Rare Hereditary Thrombophilia

Drugs & Therapeutics for Rare Hereditary Thrombophilia

Search Clinical Trials , NIH Clinical Center for Rare Hereditary Thrombophilia

Genetic Tests for Rare Hereditary Thrombophilia

Anatomical Context for Rare Hereditary Thrombophilia

MalaCards organs/tissues related to Rare Hereditary Thrombophilia:

40
Bone

Publications for Rare Hereditary Thrombophilia

Articles related to Rare Hereditary Thrombophilia:

# Title Authors PMID Year
1
Multifactorial Painful Leg Ulcers Due to Hyperhomocysteinemia, Plasminogen Activator Inhibitor-1 4G/5G Heterozygote Gene Mutation, and Beta Thalassemia Minor: A Case Report. 61
31409160 2019
2
Prevention, management and extent of adverse pregnancy outcomes in women with hereditary antithrombin deficiency. 61
23999648 2014

Variations for Rare Hereditary Thrombophilia

Expression for Rare Hereditary Thrombophilia

Search GEO for disease gene expression data for Rare Hereditary Thrombophilia.

Pathways for Rare Hereditary Thrombophilia

GO Terms for Rare Hereditary Thrombophilia

Sources for Rare Hereditary Thrombophilia

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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