Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandBlood Coagulation Disorders, Inherited (D025861)
Parent Node:
expandCoagulation Protein Disorders (D020147)
Parent Node:
expandHemorrhagic Disorders (D006474)
..Starting node
..expandFactor XIII Deficiency (D005177)

       Child Nodes:
........expandFactor Xiii, A Subunit, Deficiency Of (C567691)
........expandFactor XIII, B Subunit, Deficiency Of (C567688)



 Sister Nodes: 
..expandAfibrinogenemia (D000347) Child3
..expandAlbinism with hemorrhagic diathesis and pigmented reticuloendothelial cells (C538539)
..expandAnti-plasmin deficiency, congenital (C537777)
..expandAntithrombin, Familial Hemorrhagic Diathesis due to (C565947)
..expandBernard-Soulier Syndrome (D001606) Child5
..expandDisseminated Intravascular Coagulation (D004211)
..expandFactor V Deficiency (D005166) Child4
..expandFactor VII Deficiency (D005168)
..expandFactor X Deficiency (D005171)
..expandFactor XI Deficiency (D005173)
..expandFactor XII Deficiency (D005175)
..expandFactor XIII Deficiency (D005177) Child2
..expandHemophilia A (D006467) Child5
..expandHemophilia B (D002836)
..expandHEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION, AND CATARACTS (OMIM:613730)
..expandHemostatic Disorders (D020141) Child48
..expandHypoprothrombinemias (D007020) Child2
..expandPlasminogen Activator Inhibitor-1 Deficiency (C567640)
..expandPlatelet Storage Pool Deficiency (D010981) Child5
..expandPurpura, Thrombocytopenic, Idiopathic (D016553)
..expandThrombasthenia (D013915) Child3
..expandThrombocythemia, Essential (D013920)
..expandVitamin K Deficiency (D014813) Child1
..expandvon Willebrand Diseases (D014842) Child6
..expandWaterhouse-Friderichsen Syndrome (D014884) Child1
..expandWiskott-Aldrich Syndrome (D014923) Child1
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:4109
Name:Factor XIII Deficiency
Definition:A deficiency of blood coagulation FACTOR XIII or fibrin stabilizing factor (FSF) that prevents blood clot formation and results in a clinical hemorrhagic diathesis.
Alternative IDs:
ParentIDs:MESH:D006474|MESH:D020147|MESH:D025861
TreeNumbers:C15.378.100.100.335 |C15.378.100.141.335 |C15.378.463.335 |C16.320.099.335
Synonyms:Deficiencies, Factor XIII |Deficiency, Factor XIII |Factor XIII Deficiencies
Slim Mappings:Blood disease|Genetic disease (inborn)
Reference: MedGen: D005177
MeSH: D005177
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants