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Identifiant pérenne de la notice : 064826074Copier cet identifiant (PPN)
Notice de type FMeSH

Point d'accès autorisé

Maladies génétiques congénitales

Variantes de point d'accès

Disease, Inborn Genetic
[Nom commun]
Diseases, Inborn Genetic
[Nom commun]
Genetic Disease, Inborn
[Nom commun]
Inborn Genetic Disease
[Nom commun]
Inborn Genetic Diseases
[Nom commun]
Génopathies
[Nom commun]
Hereditary Diseases
[Nom commun]
Hereditary Disease
[Nom commun]
Disease, Hereditary
[Nom commun]
Diseases, Hereditary
[Nom commun]
Genetic Disorders
[Nom commun]
Disorder, Genetic
[Nom commun]
Disorders, Genetic
[Nom commun]
Genetic Disorder
[Nom commun]
Genetic Diseases
[Nom commun]
Disease, Genetic
[Nom commun]
Diseases, Genetic
[Nom commun]
Genetic Disease
[Nom commun]
Single-Gene Defects
[Nom commun]
Defect, Single-Gene
[Nom commun]
Defects, Single-Gene
[Nom commun]
Single Gene Defects
[Nom commun]
Single-Gene Defect
[Nom commun]
Maladies héréditaires
[Nom commun]
Maladie héréditaire
[Nom commun]
Anomalies monogéniques
[Nom commun]
Génopathies monogéniques
[Nom commun]
Maladies monogéniques
[Nom commun]
Génopathies
[Nom commun]

Informations

Note publique d''information : 
Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero

Note publique d''information : 
Diseases caused by genetic mutations that are inherited from a parent's genome

Note générale sur le champ d'application : 
general; prefer /genet with specific diseases


Notice d'autorité liée

Point d'accès autorisé parallèle

Genetic Diseases, Inborn

Identifiants externes

Identifiant MeSH : mesD030342

Utilisation dans FMeSH

Qualificatifs autorisés : DI / PS / IM / MI / DG / PP / RH / EN / ET / MO / EP / BL / CF / CI / DH / DT / TH / PX / UR / VI / VE / HI / CL / EC / EM / GE / NU / RT / EH / PC / PA / ME / CO / SU2002

... Références liées : ...