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loading...| Preferred Name |
Congenital_Systemic_Disorder |
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| Synonyms |
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|
| ID |
http://www.owl-ontologies.com/Ontology1358660052.owl#Congenital_Systemic_Disorder |
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| ID |
C97151 |
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| NCI_Definition |
An inherited disorder that presents with systemic manifestations. |
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| NCI_PT |
Congenital Systemic Disorder |
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| NICHD_Definition |
An inherited disorder that affects in multiple tissue types or in multiple organ systemsis, or affects the body as a whole. |
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| prefixIRI |
Congenital_Systemic_Disorder |
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| prefLabel |
Congenital_Systemic_Disorder |
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| Subset_Association1 | ||
| Subset_Association2 |
NICHD Pediatric Terminology |
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| SYN | ||
| subClassOf |
http://www.owl-ontologies.com/Ontology1358660052.owl#Congenital_Abnormality |
Create mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C97151 | NCIT | LOOM | |
| http://purl.obolibrary.org/obo/NCIT_C97151 | BERO | LOOM |