Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
Click a node to open it in a new tab
Disease: 1Symptom: 1Target: 1Links: 2
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 18713
- Core Entity Id
- 77153
- Source Entity Count
- 1
- Preferred Name
- Spinocerebellar Ataxia, Autosomal Recessive 14
- Name Cn
- 脊髓小脑性共济失调，常染色体隐性遗传14型
- Name Pinyin
- Ji Sui Xiao Nao Xing Gong Ji Shi Tiao ， Chang Ran Se Ti Yin Xing Yi Chuan 14 Xing
- Name En
- Spinocerebellar Ataxia, Autosomal Recessive 14
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Do Class
- disease of anatomical entity; genetic disease
- Hpo Class
- Mesh Class Name
- Hpo Class Name
- Do Class Name
- genetic disease; disease of anatomical entity
- Disease Definition
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Spinocerebellar Ataxia, Autosomal Recessive 14
Role
preferred
Name
Autosomal Recessive Spinocerebellar Ataxia 14
Role
alias
Name
CEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE, SPECTRIN-ASSOCIATED, 1
Role
alias
Name
SCAR14
Role
alias
Name
SPARCA1
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS022339
Omim
615386
Umls
C3809327
Sym Map
SMDE04218
Do Class
DOID:630DOID:7
Dis Ge Net
C3809327
Umls Sty
T047
Tcmbank Disease
5951
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Do Class Name
genetic disease; disease of anatomical entity
Disease Type
disease
Do Disease Class
disease of anatomical entity; genetic disease
Umls Disease Type
Disease or Syndrome
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome