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Identifiant IdRef : 040671852
Notice de type FMeSH

Point d'accès autorisé

Troubles de l'hémostase et de la coagulation

Variantes de point d'accès

Disorders, Blood Coagulation
[Nom commun]
Coagulation Disorders, Blood
[Nom commun]
Blood Coagulation Disorder
[Nom commun]
Coagulation Disorder, Blood
[Nom commun]
Disorder, Blood Coagulation
[Nom commun]
Coagulopathies
[Nom commun]
Troubles de la coagulation sanguine
[Nom commun]
Coagulopathies
[Nom commun]
Troubles de la coagulation sanguine
[Nom commun]

Informations

Note publique d''information : 
Hemorrhagic and thrombotic disorders that occur as a consequence of abnormalities in blood coagulation due to a variety of factors such as COAGULATION PROTEIN DISORDERS; BLOOD PLATELET DISORDERS; BLOOD PROTEIN DISORDERS or nutritional conditions

Note générale sur le champ d'application : 
GEN: prefer specifics; consider also COAGULATION PROTEIN DISORDERS and indentions; see also THROMBOSIS; EMBOLISM and specifics in C14; /genet: consider also BLOOD COAGULATION DISORDERS, INHERITED; DF: BLOOD COAG DIS

Point d'accès autorisé parallèle

Blood Coagulation Disorders

Autres identifiants

Identifiant MeSH : mesD001778

Utilisation dans FMeSH

Qualificatifs autorisés : PS / IM / MI / DI / DG / PP / RH / EN / ET / MO / EP / PC / BL / CF / CI / CN / DH / DT / TH / PX / UR / VI / VE / HI / CL / CO / EC / EM / GE / ME / NU / RT / SU / EH / PA

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