The way property values are displayed:
The way concept relations are shown:
The way concept relations are shown:
Genetic Diseases, Inborn
Hierarchy: | ∟ ∟ Genetic Diseases, Inborn 3 coordinate concepts35 subordinate conceptsX |
Broader terms: | |
Narrower terms: | |
Annotation: | GEN only: prefer /genet with specific diseases; Manual 23.22+; Manual 19.8.34
X |
historyNote*: | 2002
X |
publicMeSHNote*: | 2002; for HEREDITARY DISEASES see HEREDITARY DISEASES 1968-2001
X |
Scope note: | 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.
X |
activeMeSHYear*: | |
dateCreated*: | 2001-07-25X |
dateEstablished*: | 2002-01-01X |
dateRevised*: | 2002-07-03X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | jmpX |
recordOriginator*: | nnsX |
Related term: | |
Type: | |
Coordinate terms: | |
URI: | |
Labels and equivalent concepts: | Perinnölliset sairaudet (fi) XInborn Genetic Diseases (en, replaced) Hereditary Disease (en, replaced) Enfermedades Genéticas Congénitas (es) Genetische Krankheiten, angeborene (de) genetické nemoci vrozené (cs) Enfermedades Hereditarias (es, replaced) Hereditäre Krankheiten (de, replaced) Erbkrankheiten (de, replaced) |
Share: |
Loading results...