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Identifiant IdRef : 040844951Copier cet identifiant (PPN)
Notice de type FMeSH

Point d'accès autorisé

Hyperhomocystéinémie

Variante de point d'accès

Hyperhomocysteinemias
[Nom commun]

Informations

Note publique d''information : 
Condition in which the plasma levels of homocysteine and related metabolites are elevated (>13.9 μmol/l). Hyperhomocysteinemia can be familial or acquired. Development of the acquired hyperhomocysteinemia is mostly associated with vitamins B and/or folate deficiency (e.g., PERNICIOUS ANEMIA, vitamin malabsorption). Familial hyperhomocysteinemia often results in a more severe elevation of total homocysteine and excretion into the urine, resulting in HOMOCYSTINURIA. Hyperhomocysteinemia is a risk factor for cardiovascular and neurodegenerative diseases, osteoporotic fractures and complications during pregnancy

Point d'accès autorisé parallèle

Hyperhomocysteinemia

Autres identifiants

Identifiant MeSH : mesD020138

Utilisation dans FMeSH

Qualificatifs autorisés : DI / PS / IM / MI / DG / PP / RH / EN / ET / MO / EP / BL / CF / CI / CN / DH / DT / TH / PX / UR / VI / VE / HI / CL / CO / EC / EM / GE / NU / RT / SU / EH / PC / PA / ME1999

Equivalent dans un autre référentiel

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