DiseaseID 17527

家族性裂脑畸形

disease

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Relationship Network

Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.

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Disease: 1Symptom: 4Target: 12Links: 16
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Record Fields

Scalar fields from the final disease record.

Disease Id
17527
Core Entity Id
75774
Source Entity Count
1
Preferred Name
Familial Schizencephaly
Name Cn
家族性裂脑畸形
Name Pinyin
Jia Zu Xing Lie Nao Ji Xing
Name En
Familial Schizencephaly
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Do Class
Hpo Class
Mesh Class Name
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Hpo Class Name
Do Class Name
Disease Definition
Version
v2
Suppressed
No

Names

Preferred names, aliases, and source labels retained in the final schema.

Name
Familial Schizencephaly
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS020381
Umls
C2931870
Sym Map
SMDE08652
Dis Ge Net
C2931870
Umls Sty
T047
Me Sh Class
C10C16
Tcmbank Disease
26157

Attributes

Merged source attributes and domain-specific metadata.

Version
v2
Suppress
0
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Umls Semantic Type Name
Disease or Syndrome