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