Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Symptom: 1Target: 1Links: 2
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 17780
- Core Entity Id
- 76075
- Source Entity Count
- 1
- Preferred Name
- Ataxia, Spastic, Childhood-Onset, Autosomal Recessive, With Optic Atrophy And Mental Retardation
- Name Cn
- 儿童期起病的常染色体隐性痉挛性共济失调伴视神经萎缩和智力低下
- Name Pinyin
- Er Tong Qi Qi Bing De Chang Ran Se Ti Yin Xing Jing Luan Xing Gong Ji Shi Tiao Ban Shi Shen Jing Wei Suo He Zhi Li Di Xia
- Name En
- Ataxia, Spastic, Childhood-Onset, Autosomal Recessive, With Optic Atrophy And Mental Retardation
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Do Class
- Hpo Class
- Mesh Class Name
- Hpo Class Name
- Do Class Name
- Disease Definition
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Ataxia, Spastic, Childhood-Onset, Autosomal Recessive, With Optic Atrophy And Mental Retardation
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS020847
Omim
270500
Umls
C3151619
Sym Map
SMDE06106
Dis Ge Net
C3151619
Umls Sty
T047
Tcmbank Disease
10746
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome