DiseaseID 4589
脑脊膜膨出
disease
MSH2017_2016_08_12:A congenital or acquired protrusion of the meninges, unaccompanied by neural tissue, through a bony defect in the skull or vertebral column.|HPO2016_07_04:Protrusion of the meninges through a defect of
Relationship Network
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Disease: 1Symptom: 6Target: 10Links: 16
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 4589
- Core Entity Id
- 60961
- Source Entity Count
- 1
- Preferred Name
- Meningocele
- Name Cn
- 脑脊膜膨出
- Name Pinyin
- Nao Ji Mo Peng Chu
- Name En
- Meningocele
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Congenital Abnormality
- Disgenet Type
- disease
- Mesh Class
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and SymptomsMusculoskeletal Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
- Do Class
- physical disorder
- Hpo Class
- Abnormality of the nervous system
- Mesh Class Name
- Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System DiseasesPathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
- Hpo Class Name
- Abnormality of the nervous system
- Do Class Name
- physical disorder
- Disease Definition
- MSH2017_2016_08_12:A congenital or acquired protrusion of the meninges, unaccompanied by neural tissue, through a bony defect in the skull or vertebral column.|HPO2016_07_04:Protrusion of the meninges through a defect of the vertebral column. [HPO:sdoelken]
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Meningocele
Role
preferred
Name
Congenital Meningocele
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0002435
Herb
HBDIS001916HBDIS012861
Me Sh
D008588
Umls
C0025299C1261470
Sym Map
SMDE07473SMDE10861
Do Class
DOID:0080015
Dis Ge Net
C0025299C1261470
Umls Sty
T019T047
Hpo Class
HP:0000707
Me Sh Class
C05C10C16C23
Tcmbank Disease
1789519676
Itcmdb Generated
ITX-DISEASE-5C8C493DD2CB
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Do Class Name
physical disorder
Disease Type
disease
Hpo Class Name
Abnormality of the nervous system
Do Disease Class
physical disorder
Hpo Disease Class
Abnormality of the nervous system
Umls Disease Type
Congenital AbnormalityDisease or Syndrome
Disease Definition
MSH2017_2016_08_12:A congenital or acquired protrusion of the meninges, unaccompanied by neural tissue, through a bony defect in the skull or vertebral column.|HPO2016_07_04:Protrusion of the meninges through a defect of the vertebral column. [HPO:sdoelken]NCI2016_02D:A congenital abnormality in which the meninges protrude through a defect in the spinal column or the cranium.
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and SymptomsMusculoskeletal Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System DiseasesPathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Umls Semantic Type Name
Congenital AbnormalityDisease or Syndrome