Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Target: 19Links: 24
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 32555
- Core Entity Id
- 192489
- Source Entity Count
- 1
- Preferred Name
- Holoprosencephaly-Caudal Dysgenesis Syndrome
- Name Cn
- 前脑无裂畸形-尾部发育不全综合征
- Name Pinyin
- Qian Nao Wu Lie Ji Xing - Wei Bu Fa Yu Bu Quan Zong He Zheng
- Name En
- Holoprosencephaly-Caudal Dysgenesis 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
- Version
- Suppressed
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Holoprosencephaly-Caudal Dysgenesis Syndrome
Role
preferred
Source
ETCM_v2
Preferred
Yes
Cross References
Trusted external identifiers retained for this final record.
Etcm Disease
Holoprosencephaly-Caudal Dysgenesis Syndrome
Itcmdb Generated
ITX-DISEASE-5BEB6DDDD655
Attributes
Merged source attributes and domain-specific metadata.
Page Title
Disease Holoprosencephaly-Caudal Dysgenesis Syndrome Details page
Basic Information
Disease Name
Holoprosencephaly-Caudal Dysgenesis Syndrome
Global Category
Fetal diseases;Rare diseases
Anatomical Category
Neuronal diseases