Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Symptom: 2Target: 1Links: 3
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 16453
- Core Entity Id
- 74530
- Source Entity Count
- 1
- Preferred Name
- Pontocerebellar Hypoplasia Type 6
- Name Cn
- 桥小脑发育不全6型
- Name Pinyin
- Qiao Xiao Nao Fa Yu Bu Quan 6 Xing
- Name En
- Pontocerebellar Hypoplasia Type 6
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- 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
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
- Hpo Class Name
- Do Class Name
- disease of anatomical entity
- Disease Definition
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Pontocerebellar Hypoplasia Type 6
Role
preferred
Name
Pontocerebellar Hypoplasia, Type 6
Role
preferred
Name
ENCEPHALOPATHY, FATAL INFANTILE, WITH MITOCHONDRIAL RESPIRATORY CHAIN DEFECTS
Role
alias
Name
PCH6
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS018729
Omim
611523
Umls
C1969084
Sym Map
SMDE02748
Do Class
DOID:7
Dis Ge Net
C1969084
Umls Sty
T019T047
Me Sh Class
C10C16
Tcmbank Disease
15383
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Do Class Name
disease of anatomical entity
Disease Type
disease
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
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Umls Semantic Type Name
Disease or Syndrome; Congenital Abnormality