loading...| Preferred Name |
Connective Tissue Disorder |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C26729 |
| ALT_DEFINITION |
A heterogeneous group of disorders, some hereditary, others acquired, characterized by abnormal structure or function of one or more of the elements of connective tissue, i.e., collagen, elastin, or the mucopolysaccharides. A disorder characterized by abnormalities in one or more of the elements of the connective tissues, typically associated with genetic defects. |
| code |
C26729 |
| Concept_In_Subset |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C118468 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C90259 |
| Contributing_Source |
NICHD FDA |
| DEFINITION |
A non-neoplastic or neoplastic disorder that affects the connective tissue. |
| FDA_Table |
Patient Code (Appendix B) |
| FULL_SYN |
Tissue Disease, Connective Connective Tissue Disorders Connective Tissue Disease Disorder of Connective Tissue Primary Disorder of Connective Tissue Disease, Connective Tissue Connective Tissue Diseases |
| Has_CDRH_Parent | |
| Has_NICHD_Parent | |
| label |
Connective Tissue Disorder |
| Legacy_Concept_Name |
Connective_Tissue_Disorder |
| NICHD_Hierarchy_Term |
Connective Tissue Disorder |
| Preferred_Name |
Connective Tissue Disorder |
| prefixIRI |
C26729 |
| prefLabel |
Connective Tissue Disorder |
| Semantic_Type |
Disease or Syndrome |
| UMLS_CUI |
C0009782 |
| subClassOf |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| There are currently no mappings for this class. | |||