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: 2Target: 17Links: 26
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 26196
- Core Entity Id
- 118764
- Source Entity Count
- 1
- Preferred Name
- Craniodiaphyseal Dysplasia, Autosomal Dominant
- Name Cn
- 常染色体显性遗传颅骨骨干发育不良
- Name Pinyin
- Chang Ran Se Ti Xian Xing Yi Chuan Lu Gu Gu Gan Fa Yu Bu Liang
- Name En
- Craniodiaphyseal Dysplasia, Autosomal Dominant
- 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
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Craniodiaphyseal Dysplasia, Autosomal Dominant
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Umls
C2675746
Sym Map
SMDE02360
Etcm Disease
Craniodiaphyseal Dysplasia, Autosomal Dominant
Itcmdb Generated
ITX-DISEASE-299AC4B3B36B
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Page Title
Disease Craniodiaphyseal Dysplasia, Autosomal Dominant Details page
Basic Information
Disease Name
Craniodiaphyseal Dysplasia, Autosomal Dominant
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Bone diseases