DiseaseID 17562

局灶性皮质发育不良

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: 1Target: 3Links: 3
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Record Fields

Scalar fields from the final disease record.

Disease Id
17562
Core Entity Id
75819
Source Entity Count
1
Preferred Name
Focal Cortical Dysplasia
Name Cn
局灶性皮质发育不良
Name Pinyin
Ju Zao Xing Pi Zhi Fa Yu Bu Liang
Name En
Focal Cortical Dysplasia
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
Abnormality of the nervous system
Mesh Class Name
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Hpo Class Name
Abnormality of the nervous system
Do Class Name
Disease Definition
Version
Suppressed

Names

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

Name
Focal Cortical Dysplasia
Role
preferred
Name
Focal Cortical Dysplasia Is One of The Most Common Entities Associated With Refractory Epilepsy, Especially In Childhood.
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Hpo
HP:0032046
Herb
HBDIS020472
Dis Ge Net
C2938983
Umls Sty
T047
Hpo Class
HP:0000707
Me Sh Class
C10C16
Tcmbank Disease
18176

Attributes

Merged source attributes and domain-specific metadata.

Disease Type
disease
Hpo Class Name
Abnormality of the nervous system
Hpo Disease Class
Abnormality of the nervous system
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