Preferred Label : genetic mutation;
Origin ID : F-E1950;
UMLS CUI : C0026882;
SNOMED CT concept
Semantic type(s)
UMLS correspondences (same concept)
http://www.theses.fr/2019LIL2S016
2019
France
dissertations, academic
genetic diseases, inborn
mutation
hereditary disease, nos
genetic mutation
Researches
Genetics
Diseases
Genetics
Genetic disease
genetic research
crohn disease
crohn's disease, nos
Genetics
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