Preferred Name | Osteogenesis_Imperfecta | |
Synonyms |
|
|
ID |
http://www.owl-ontologies.com/Ontology1358660052.owl#Osteogenesis_Imperfecta |
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ID |
C26837 |
|
NCI_Definition |
A group of usually autosomal dominant inherited disorders characterized by defective synthesis of collagen type I resulting in defective collagen formation. It is characterized by brittle and easily fractured bones. |
|
NCI_PT |
Osteogenesis Imperfecta |
|
NICHD_Definition |
_ |
|
prefixIRI |
Osteogenesis_Imperfecta |
|
prefLabel |
Osteogenesis_Imperfecta |
|
Subset_Association1 |
NICHD Pediatric Terminology |
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Subset_Association2 |
Neonatal Research Network Terminology |
|
SYN |
Congenital Anomaly of Skeletal Bone |
|
subClassOf |
http://www.owl-ontologies.com/Ontology1358660052.owl#Metabolic_Disease_of_Collagen |
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