Coronavirus Infectious Disease Ontology

Last uploaded: February 16, 2024
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

http://evs.nci.nih.gov/ftp1/NDF-RT/NDF-RT.owl

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

http://evs.nci.nih.gov/ftp1/NDF-RT/NDF-RT.owl#N0000002121

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