DiseaseID 32011
先天性肌张力低下、癫痫、发育迟缓和指趾畸形
Congenital Hypotonia, Epilepsy, Developmental Delay, and Digital Anomalies
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Herb: 5Target: 17Links: 29
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 32011
- Core Entity Id
- 191945
- Source Entity Count
- 1
- Preferred Name
- Congenital Hypotonia, Epilepsy, Developmental Delay, and Digital Anomalies
- Name Cn
- 先天性肌张力低下、癫痫、发育迟缓和指趾畸形
- Name Pinyin
- Xian Tian Xing Ji Zhang Li Di Xia 、 Dian Xian 、 Fa Yu Chi Huan He Zhi Zhi Ji Xing
- Name En
- Congenital Hypotonia, Epilepsy, Developmental Delay, and Digital Anomalies
- 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
- Suppressed
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Congenital Hypotonia, Epilepsy, Developmental Delay, and Digital Anomalies
Role
preferred
Source
ETCM_v2
Preferred
Yes
Cross References
Trusted external identifiers retained for this final record.
Etcm Disease
Congenital Hypotonia, Epilepsy, Developmental Delay, and Digital Anomalies
Itcmdb Generated
ITX-DISEASE-20361A97B260
Attributes
Merged source attributes and domain-specific metadata.
Page Title
Disease Congenital Hypotonia, Epilepsy, Developmental Delay, and Digital Anomalies Details page
Basic Information
Disease Name
Congenital Hypotonia, Epilepsy, Developmental Delay, and Digital Anomalies
Global Category
Genetic diseases
Anatomical Category
Bone diseases;Neuronal diseases