Statements (56)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
medical specialty
|
| gptkbp:associatedWith |
intellectual disability
rare diseases hereditary cancer syndromes congenital anomalies mitochondrial disorders X-linked disorders autosomal dominant disorders autosomal recessive disorders multifactorial diseases |
| gptkbp:focusesOn |
diagnosis of genetic disorders
management of genetic disorders prevention of genetic disorders |
| gptkbp:governedBy |
gptkb:American_Board_of_Medical_Genetics_and_Genomics
European Board of Medical Genetics |
| https://www.w3.org/2000/01/rdf-schema#label |
Clinical Genetics
|
| gptkbp:involves |
genetic counseling
genetic testing risk assessment family history analysis |
| gptkbp:practicedIn |
clinical geneticists
|
| gptkbp:publishedIn |
gptkb:American_Journal_of_Medical_Genetics
gptkb:Genetics_in_Medicine Clinical Genetics (journal) European Journal of Human Genetics |
| gptkbp:relatedTo |
genomics
medical genetics obstetrics oncology pediatrics |
| gptkbp:specialty |
cancer genetics
neurogenetics pediatric genetics adult genetics cardiogenetics metabolic genetics prenatal genetics reproductive genetics |
| gptkbp:usedFor |
pharmacogenomics
personalized medicine carrier screening newborn screening prenatal diagnosis identifying inherited diseases |
| gptkbp:uses |
gptkb:polymerase_chain_reaction
gptkb:Sanger_sequencing gptkb:fluorescence_in_situ_hybridization next-generation sequencing cytogenetic analysis whole genome sequencing whole exome sequencing molecular genetic testing chromosomal microarray analysis biochemical genetic testing |
| gptkbp:bfsParent |
gptkb:Medical_Genetics
|
| gptkbp:bfsLayer |
7
|