DiseaseID 2307

胎儿起病的橄榄体脑桥小脑发育不全

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: 1Links: 1
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Record Fields

Scalar fields from the final disease record.

Disease Id
2307
Core Entity Id
2597
Source Entity Count
1
Preferred Name
Olivopontocerebellar Hypoplasia, Fetal-Onset
Name Cn
胎儿起病的橄榄体脑桥小脑发育不全
Name Pinyin
Tai Er Qi Bing De Gan Lan Ti Nao Qiao Xiao Nao Fa Yu Bu Quan
Name En
Olivopontocerebellar Hypoplasia, Fetal-Onset
Name Latin
Bilingual Status
complete
Disease Type
Umls Disease Type
Disease or Syndrome; Congenital Abnormality
Disgenet Type
disease
Mesh Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Do Class
disease of anatomical entity
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
Olivopontocerebellar Hypoplasia, Fetal-Onset
Role
preferred
Name
Pontocerebellar Hypoplasia, Type 5
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS028958
Omim
610204
Do Class
DOID:7
Dis Ge Net
C1857762
Umls Sty
T019T047
Me Sh Class
C10C16

Attributes

Merged source attributes and domain-specific metadata.

Do Disease Class
disease of anatomical entity
Umls Disease Type
Disease or Syndrome; Congenital Abnormality
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Dis Ge Net Disease Type
disease