Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Formula: 12Herb: 1Target: 17Links: 37
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 31737
- Core Entity Id
- 191671
- Source Entity Count
- 1
- Preferred Name
- Autosomal Recessive Ataxia Due to Pex10 Deficiency
- Name Cn
- PEX10缺陷所致常染色体隐性共济失调
- Name Pinyin
- Pex10 Que Xian Suo Zhi Chang Ran Se Ti Yin Xing Gong Ji Shi Tiao
- Name En
- Autosomal Recessive Ataxia Due to Pex10 Deficiency
- Name Latin
- Bilingual Status
- complete
- Disease Type
- Umls Disease Type
- Disgenet Type
- Mesh Class
- Do Class
- 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
Autosomal Recessive Ataxia Due to Pex10 Deficiency
Role
preferred
Source
ETCM_v2
Preferred
Yes
Cross References
Trusted external identifiers retained for this final record.
Etcm Disease
Autosomal Recessive Ataxia Due to Pex10 Deficiency
Itcmdb Generated
ITX-DISEASE-F03E4CB18551
Attributes
Merged source attributes and domain-specific metadata.
Page Title
Disease Autosomal Recessive Ataxia Due to Pex10 Deficiency Details page
Basic Information
Disease Name
Autosomal Recessive Ataxia Due to Pex10 Deficiency
Global Category
Rare diseases
Anatomical Category
Neuronal diseases