Preferred Name | Genetic Marker | |
Synonyms |
|
|
Definitions |
A segment of DNA with an identifiable physical location on a chromosome and whose inheritance can be followed. |
|
ID |
http://purl.obolibrary.org/obo/NCIT_C16622 |
|
ALT_DEFINITION |
Alteration in DNA that may indicate an increased risk of developing a specific disease or disorder. |
|
code |
C16622 |
|
definition |
A segment of DNA with an identifiable physical location on a chromosome and whose inheritance can be followed. |
|
label |
Genetic Marker |
|
Legacy Concept Name |
Genetic_Marker |
|
Preferred_Name |
Genetic Marker |
|
prefixIRI |
NCIT:C16622 |
|
prefLabel |
Genetic Marker |
|
Semantic_Type |
Nucleotide Sequence |
|
UMLS_CUI |
C0017393 |
|
subClassOf |
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