DiseaseID 26304
I型成骨不全症
Osteogenesis Imperfecta, Type I
NCI2016_02D:The mildest and most common type of osteogenesis imperfecta. It is characterized by bone fractures, muscle weakness, and loose joints. Bone deformities are either absent or minimal.
Relationship Network
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Disease: 1Symptom: 5Target: 5Links: 10
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 26304
- Core Entity Id
- 118872
- Source Entity Count
- 1
- Preferred Name
- Osteogenesis Imperfecta, Type I
- Name Cn
- I型成骨不全症
- Name Pinyin
- I Xing Cheng Gu Bu Quan Zheng
- Name En
- Osteogenesis Imperfecta, Type I
- 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:The mildest and most common type of osteogenesis imperfecta. It is characterized by bone fractures, muscle weakness, and loose joints. Bone deformities are either absent or minimal.
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Osteogenesis Imperfecta, Type I
Role
preferred
Source
SymMap_v2
Preferred
Yes
Cross References
Trusted external identifiers retained for this final record.
Umls
C0023931
Sym Map
SMDE02898
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Disease Definition
NCI2016_02D:The mildest and most common type of osteogenesis imperfecta. It is characterized by bone fractures, muscle weakness, and loose joints. Bone deformities are either absent or minimal.