Preferred Name | Osteogenesis Imperfecta | |
Synonyms |
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|
Definitions |
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. |
|
ID |
http://purl.obolibrary.org/obo/NCIT_C26837 |
|
ALT_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. |
|
code |
C26837 |
|
Contributing_Source |
Cellosaurus ACC/AHA NICHD |
|
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. |
|
in_subset |
http://purl.obolibrary.org/obo/NCIT_C90259 http://purl.obolibrary.org/obo/NCIT_C165258 |
|
label |
Osteogenesis Imperfecta |
|
Legacy Concept Name |
Osteogenesis_Imperfecta |
|
Preferred_Name |
Osteogenesis Imperfecta |
|
prefixIRI |
NCIT:C26837 |
|
prefLabel |
Osteogenesis Imperfecta |
|
Semantic_Type |
Disease or Syndrome |
|
UMLS_CUI |
C0029434 |
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subClassOf |