DiseaseID 26223
骨硬化-发育迟缓-颅缝早闭综合征
Osteosclerosis-Developmental Delay-Craniosynostosis Syndrome
This newly described syndrome is characterized by osteosclerosis, developmental delay and craniosynostosis (see this term).
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Disease: 1Symptom: 5Target: 1Links: 6
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 26223
- Core Entity Id
- 118791
- Source Entity Count
- 1
- Preferred Name
- Osteosclerosis-Developmental Delay-Craniosynostosis Syndrome
- Name Cn
- 骨硬化-发育迟缓-颅缝早闭综合征
- Name Pinyin
- Gu Ying Hua - Fa Yu Chi Huan - Lu Feng Zao Bi Zong He Zheng
- Name En
- Osteosclerosis-Developmental Delay-Craniosynostosis Syndrome
- 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
- This newly described syndrome is characterized by osteosclerosis, developmental delay and craniosynostosis (see this term).
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Osteosclerosis-Developmental Delay-Craniosynostosis Syndrome
Role
preferred
Source
SymMap_v2
Preferred
Yes
Cross References
Trusted external identifiers retained for this final record.
Sym Map
SMDE02480
Orphanet
178377
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Disease Definition
This newly described syndrome is characterized by osteosclerosis, developmental delay and craniosynostosis (see this term).