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loading...| Preferred Name | Congenital_Connective_Tissue_Disorder | |
| Synonyms |
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|
| ID |
http://www.owl-ontologies.com/Ontology1358660052.owl#Congenital_Connective_Tissue_Disorder |
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| ID |
C97075 |
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| NCI_Definition |
An inherited genetic disorder that affects the connective tissues. Representative examples include Ehlers-Danlos syndrome and Marfan syndrome. |
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| NCI_PT |
Hereditary Connective Tissue Disorder |
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| NICHD_Definition |
_ |
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| prefixIRI |
Congenital_Connective_Tissue_Disorder |
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| prefLabel |
Congenital_Connective_Tissue_Disorder |
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| Subset_Association1 |
NICHD Pediatric Terminology |
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| Subset_Association2 |
Neonatal Research Network Terminology |
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| SYN |
Connective Tissue Hereditary Disorder |
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| subClassOf |
http://www.owl-ontologies.com/Ontology1358660052.owl#Congenital_Abnormality |
Create mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/MEDDRA/10086687 | MEDDRA | LOOM | |
| http://purl.bioontology.org/ontology/SNOMEDCT/363039000 | SNOMEDCT | LOOM |