Preferred Name |
Genetic Diseases, Inborn [Disease/Finding] |
|
Synonyms |
|
|
ID |
http://evs.nci.nih.gov/ftp1/NDF-RT/NDF-RT.owl#N0000011105 |
|
code |
C291458 |
|
Display_Name |
Genetic Diseases, Inborn |
|
imported from | ||
label |
Genetic Diseases, Inborn [Disease/Finding] |
|
MeSH_CUI |
M0385531 |
|
MeSH_Definition |
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. |
|
MeSH_DUI |
D030342 |
|
MeSH_Name |
Genetic Diseases, Inborn |
|
NUI |
N0000011105 |
|
prefixIRI |
NDF-RT:N0000011105 |
|
prefLabel |
Genetic Diseases, Inborn [Disease/Finding] |
|
RxNorm_CUI |
1025368 |
|
Synonym |
Inborn Genetic Diseases |
|
UMLS_CUI |
C0950123 |
|
subClassOf |
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