DiseaseID 25803
Eiken综合征
Eiken Syndrome
Eiken syndrome is a rare familial skeletal dysplasia characterized by multiple epiphyseal dysplasia, with extremely retarded ossification. It has been described in 6 members of a unique consanguineous
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: 1Herb: 1Symptom: 1Target: 20Links: 26
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 25803
- Core Entity Id
- 118371
- Source Entity Count
- 1
- Preferred Name
- Eiken Syndrome
- Name Cn
- Eiken综合征
- Name Pinyin
- Eiken Zong He Zheng
- Name En
- Eiken 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
- Eiken syndrome is a rare familial skeletal dysplasia characterized by multiple epiphyseal dysplasia, with extremely retarded ossification. It has been described in 6 members of a unique consanguineous
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Eiken Syndrome
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Umls
C1838779
Sym Map
SMDE00413
Orphanet
79106
Etcm Disease
Eiken Syndrome
Itcmdb Generated
ITX-DISEASE-1AD78CB47972
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Page Title
Disease Eiken Syndrome Details page
Basic Information
Disease Name
Eiken Syndrome
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Bone diseases
Disease Definition
Eiken syndrome is a rare familial skeletal dysplasia characterized by multiple epiphyseal dysplasia, with extremely retarded ossification. It has been described in 6 members of a unique consanguineous