Disease Browser
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Parent Node: Blood Coagulation Disorders, Inherited (D025861) | Parent Node: Coagulation Protein Disorders (D020147) | Parent Node: Hemorrhagic Disorders (D006474) | ..Starting node ..Afibrinogenemia (D000347)
| Child Nodes:
| ........Afibrinogenemia congenital (C531603) | ........Dysfibrinogenemia, Congenital (C562727) | ........Hypodysfibrinogenemia, Congenital (C565970) |
Sister Nodes: | ..Afibrinogenemia (D000347) 3
| ..Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells (C538539)
| ..Anti-plasmin deficiency, congenital (C537777)
| ..Antithrombin, Familial Hemorrhagic Diathesis due to (C565947)
| ..Bernard-Soulier Syndrome (D001606) 5
| ..Disseminated Intravascular Coagulation (D004211)
| ..Factor V Deficiency (D005166) 4
| ..Factor VII Deficiency (D005168)
| ..Factor X Deficiency (D005171)
| ..Factor XI Deficiency (D005173)
| ..Factor XII Deficiency (D005175)
| ..Factor XIII Deficiency (D005177) 2
| ..Hemophilia A (D006467) 5
| ..Hemophilia B (D002836)
| ..HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION, AND CATARACTS (OMIM:613730)
| ..Hemostatic Disorders (D020141) 48
| ..Hypoprothrombinemias (D007020) 2
| ..Plasminogen Activator Inhibitor-1 Deficiency (C567640)
| ..Platelet Storage Pool Deficiency (D010981) 5
| ..Purpura, Thrombocytopenic, Idiopathic (D016553)
| ..Thrombasthenia (D013915) 3
| ..Thrombocythemia, Essential (D013920)
| ..Vitamin K Deficiency (D014813) 1
| ..von Willebrand Diseases (D014842) 6
| ..Waterhouse-Friderichsen Syndrome (D014884) 1
| ..Wiskott-Aldrich Syndrome (D014923) 1
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 344 |
Name: | Afibrinogenemia |
Definition: | A deficiency or absence of FIBRINOGEN in the blood. |
Alternative IDs: | |
ParentIDs: | MESH:D006474|MESH:D020147|MESH:D025861 |
TreeNumbers: | C15.378.100.100.056 |C15.378.100.141.072 |C15.378.463.067 |C16.320.099.056 |
Synonyms: | Afibrinogenemias |Congenital Afibrinogenemia |Deficiencies, Fibrinogen |Deficiency, Fibrinogen |Familial Afibrinogenemia |Fibrinogen Deficiencies |Fibrinogen Deficiency |
Slim Mappings: | Blood disease|Genetic disease (inborn) |
Reference: |
MedGen: D000347
MeSH: D000347
OMIM:
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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