MCID: RRC033
MIFTS: 11

Rare Coagulation Disorder

Categories: Blood diseases, Rare diseases

Aliases & Classifications for Rare Coagulation Disorder

MalaCards integrated aliases for Rare Coagulation Disorder:

Name: Rare Coagulation Disorder 58

Classifications:

Orphanet: 58  
Rare haematological diseases


External Ids:

UMLS via Orphanet 71 C0005779
Orphanet 58 ORPHA98429

Summaries for Rare Coagulation Disorder

MalaCards based summary : Rare Coagulation Disorder is related to factor xii deficiency and disseminated intravascular coagulation. An important gene associated with Rare Coagulation Disorder is F12 (Coagulation Factor XII).

Related Diseases for Rare Coagulation Disorder

Diseases related to Rare Coagulation Disorder via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 factor xii deficiency 9.9
2 disseminated intravascular coagulation 9.9
3 thrombophilia 9.9
4 liver cirrhosis 9.9

Symptoms & Phenotypes for Rare Coagulation Disorder

Drugs & Therapeutics for Rare Coagulation Disorder

Search Clinical Trials , NIH Clinical Center for Rare Coagulation Disorder

Genetic Tests for Rare Coagulation Disorder

Anatomical Context for Rare Coagulation Disorder

Publications for Rare Coagulation Disorder

Articles related to Rare Coagulation Disorder:

(show top 50) (show all 67)
# Title Authors PMID Year
1
Pharmacokinetics, surrogate efficacy and safety evaluations of a new human plasma-derived fibrinogen concentrate (FIB Grifols) in adult patients with congenital afibrinogenemia. 61
33486319 2021
2
Development of Acquired Factor V Inhibitor After Surgical Procedure Without the Use of Fibrin Tissue Adhesives: A Case Report. 61
33489635 2021
3
Endovenous Thermal Ablation for a Varicose Vein Patient with Factor XII Deficiency: A Case Report. 61
33391573 2020
4
Congenital Hypofibrinogenemia: Presentation of a Rare Coagulation Disorder. 61
33532157 2020
5
Antiphospholipid syndrome and valvular heart disease, a complex scenario of thrombotic events, a case report. 61
32993710 2020
6
HIV-associated and idiopathic-acquired haemophilia A: A single-centre case series from Cape Town, South Africa. 61
32641545 2020
7
Successful Treatment of Life-threatening Bleeding Caused by Acquired Factor X Deficiency Associated with Respiratory Infection. 61
32023586 2020
8
Women With Congenital Hypofibrinogenemia/Afibrinogenemia: From Birth to Death. 61
32233805 2020
9
Acquired Factor VII deficiency - a rare but important consideration. 61
31142211 2019
10
Perioperative Management of a Patient with Severe Factor V Deficiency Presenting with Chronic Subdural Hematoma: A Clinical Report. 61
30999086 2019
11
Challenges in management of unusual acquired factor V deficiency: A case report. 61
31027075 2019
12
Management of dysfibrinogenemia in pregnancy: A case report. 61
28948631 2018
13
High Titer of Acquired Factor V Inhibitor Presenting with a Pseudo-deficiency of Multiple Coagulation Factors. 61
29093398 2018
14
Diagnosis of Hypofibrinogenemia After Dental Treatment Under General Anesthesia. 61
29482685 2018
15
Factor XI deficiency and aortic valve replacement: Perioperative management. 61
27091826 2017
16
Protein S Heerlen mutation heterozygosity is associated with venous thrombosis risk. 61
28374852 2017
17
[Factor V congenital deficiency: about a case]. 61
28904709 2017
18
Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population. 61
28912669 2017
19
Successful Use of Four Factor-Prothrombin Complex Concentrate for Congenital Factor X Deficiency in the Setting of Neurosurgery. 61
27378481 2016
20
Congenital afibrinogenemia: a case report of a spontaneous hepatic hematoma. 61
27428204 2016
21
[Development of acquired hemophilia A during maintenance therapy for immune thrombocytopenia]. 61
27169450 2016
22
A 75-year-old woman with acquired haemophilia disguised by warfarin treatment. 61
26443092 2015
23
Neonatal onset of congenital factor X deficiency: a description of two novel mutations with 6-year follow-up. 61
26083982 2015
24
Coexistence of pemphigus foliaceus and acquired hemophilia A: A case report. 61
25855134 2015
25
Near fatal spontaneous intraperitoneal bleeding: A rare manifestation in a congenital factor X deficiency carrier. 61
25810617 2015
26
Managing menorrhagia in a familial case of factor V deficiency. 61
25256869 2015
27
A novel factor X gene mutation Val (GTC) 384Ala (GCC) in a Chinese family resulting in congenital factor X deficiency. 61
26309706 2015
28
Development of asymptomatic acquired factor V inhibitor after the administration of antibiotics. 61
25501413 2014
29
Spontaneous epidural and subdural hematoma in a child with afibrinogenemia and postoperative management. 61
24509337 2014
30
[An uncommon cause of hematemesis in children: factor XI deficiency]. 61
24461936 2014
31
Coagulation factor XIII deficiency. Diagnosis, prevalence and management of inherited and acquired forms. 61
24503678 2014
32
Successful living-related kidney transplantation in a boy with inherited dysfibrinogenemia. 61
23962069 2013
33
Management of factor VII-deficient patients undergoing joint surgeries--preliminary results of locally developed treatment regimen. 61
22845882 2013
34
Perioperative management of cardiac surgery patients with factor XII deficiency - two case reports. 61
23348490 2012
35
[Acquired factor V inhibitor: 3 cases report and literature review]. 61
22781721 2012
36
Functional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiency. 61
21777354 2012
37
Acute myocardial infarction in a patient with hypofibrinogenemia: a case report. 61
22182477 2011
38
Report 2 cases of congenital factor XII deficiency: a rare coagulation disorder. 61
22043782 2011
39
Epidemiology, diagnosis, and management of von Willebrand disease in India. 61
22102205 2011
40
Cellulitis on face in a patient with congenital afibrinogenemia. 61
21521918 2011
41
Anti-Factor V inhibitor in patients with autoimmune diseases: case report and literature review. 61
23754902 2011
42
Identification and functional characterization of a novel nonsense mutation in FGA accounting for congenital afibrinogenemia in six Egyptian patients. 61
20051841 2010
43
Heart valve surgery in patients with the antiphospholipid syndrome: analysis of a series of nine cases. 61
19699100 2010
44
Factor 5 mutation profile in German patients with homozygous and heterozygous factor V deficiency. 61
19486170 2009
45
Factor XI deficiency in Southern Iran: identification of a novel missense mutation. 61
18758779 2009
46
[A rare coagulation disorder. Diagnostics and management in cases of hereditary dysfibrinogenemia]. 61
19043687 2009
47
Inherited platelet function disorders versus other inherited bleeding disorders: an Indian overview. 61
17850851 2008
48
Mutational screening of six afibrinogenemic patients: identification and characterization of four novel molecular defects. 61
17393016 2007
49
[Cyclosporine A as an effective treatment for a patient with acquired hemophilia A complicated with diabetes mellitus and ischemic heart disease]. 61
16440770 2005
50
Factor XI deficiency: identification of six novel missense mutations (P23L, P69T, C92G, E243D, W497C and E547K). 61
16079124 2005

Variations for Rare Coagulation Disorder

Expression for Rare Coagulation Disorder

Search GEO for disease gene expression data for Rare Coagulation Disorder.

Pathways for Rare Coagulation Disorder

GO Terms for Rare Coagulation Disorder

Sources for Rare Coagulation Disorder

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
20 GARD
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
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
53 NINDS
54 Novoseek
56 OMIM via Orphanet
57 OMIM® (Updated 05-Apr-2021)
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 Tocris
70 UMLS
71 UMLS via Orphanet
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