DiseaseID 26740
IV型成骨不全症
Osteogenesis Imperfecta, Type Iv
NCI2016_02D:A type of osteogenesis imperfecta that is characterized by fractures and hearing loss. It is more severe than type I and less severe than types II and III.
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
Click a node to open it in a new tab
Disease: 1Symptom: 1Target: 12Links: 13
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 26740
- Core Entity Id
- 119308
- Source Entity Count
- 1
- Preferred Name
- Osteogenesis Imperfecta, Type Iv
- Name Cn
- IV型成骨不全症
- Name Pinyin
- Iv Xing Cheng Gu Bu Quan Zheng
- Name En
- Osteogenesis Imperfecta, Type Iv
- Name Latin
- Bilingual Status
- complete
- Disease Type
- Umls Disease Type
- Disgenet Type
- Mesh Class
- Do Class
- Hpo Class
- Mesh Class Name
- Hpo Class Name
- Do Class Name
- Disease Definition
- NCI2016_02D:A type of osteogenesis imperfecta that is characterized by fractures and hearing loss. It is more severe than type I and less severe than types II and III.
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Osteogenesis Imperfecta, Type Iv
Role
preferred
Source
SymMap_v2
Preferred
Yes
Cross References
Trusted external identifiers retained for this final record.
Umls
C0268363
Sym Map
SMDE04792
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Disease Definition
NCI2016_02D:A type of osteogenesis imperfecta that is characterized by fractures and hearing loss. It is more severe than type I and less severe than types II and III.