MeSH Descriptor
Source: MeSH 2021 deskriptory
Main Heading
genetické nemoci vrozené
English Heading
Genetic Diseases, Inborn
See
monogenní genetické choroby
monogenní nemoci
monogenní onemocnění
See
Genetic Disorders [T000898783]
Genetic Diseases [T000898784]
Hereditary Disease [T019715]
Hereditary Diseases [T019716]
Single-Gene Defects [T019718]
Inborn Genetic Diseases [T446732]
Related Descriptors
Preferred Concept
Mesh Scope Translators Note
Nemoci, které jsou způsobeny genetickými mutacemi přítomnými při vývoji embrya nebo plodu. Diagnostikovány mohou být později v životě. Tyto mutace mohou být zděděny z genomu rodiče nebo mohou být získány in utero.
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.
Other Concepts
Annotation
general; prefer /genet with specific diseases
History note
2002
Public Note
2002; for HEREDITARY DISEASES see HEREDITARY DISEASES 1968-2001
Record number
D030342
Persistent link
MeSH Tree


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