loading...| Preferred Name |
Hereditary Neoplastic Syndrome |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C3266 |
| ALT_DEFINITION |
Describes the clinical manifestations associated with a mutation conferring cancer susceptibility. |
| code |
C3266 |
| Concept_In_Subset |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C116977 |
| Contributing_Source |
NICHD CTRP |
| DEFINITION |
An inherited genetic condition in which members within a family are at an increased risk for the development of benign and/or malignant neoplasms. |
| Display_Name |
Hereditary Neoplastic Syndrome |
| FULL_SYN |
Familial Tumor Syndrome Familial Neoplastic Syndrome Hereditary Tumor Syndrome inherited cancer syndrome Germline Neoplastic Syndrome Hereditary Neoplastic Syndrome |
| label |
Hereditary Neoplastic Syndrome |
| Legacy Concept Name |
Hereditary_Neoplastic_Syndrome |
| Preferred_Name |
Hereditary Neoplastic Syndrome |
| prefixIRI |
Thesaurus:C3266 |
| prefLabel |
Hereditary Neoplastic Syndrome |
| Semantic_Type |
Disease or Syndrome |
| UMLS_CUI |
C0027672 |
| subClassOf |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.obolibrary.org/obo/MONDO_0015356 | Mondo Disease Ontology / Mondo疾病本体 | LOOM | |
| http://purl.obolibrary.org/obo/MONDO_0015356 | Experimental Factor Ontology / 实验性因素本体 | LOOM |