DiseaseID 18333

原发性辅酶Q10缺乏症3型

disease

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Relationship Network

Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.

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Disease: 1Symptom: 1Target: 17Links: 25
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Record Fields

Scalar fields from the final disease record.

Disease Id
18333
Core Entity Id
76717
Source Entity Count
1
Preferred Name
Coenzyme Q10 Deficiency, Primary, 3
Name Cn
原发性辅酶Q10缺乏症3型
Name Pinyin
Yuan Fa Xing Fu Mei Q10 Que Fa Zheng 3 Xing
Name En
Coenzyme Q10 Deficiency, Primary, 3
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Do Class
genetic disease; disease of metabolism
Hpo Class
Mesh Class Name
Hpo Class Name
Do Class Name
disease of metabolism; genetic disease
Disease Definition
Version
v1,v2
Suppressed
No

Names

Preferred names, aliases, and source labels retained in the final schema.

Name
Coenzyme Q10 Deficiency, Primary, 3
Role
preferred
Name
COQ10D3
Role
alias
Name
Primary Coenzyme Q10 Deficiency 3
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS021750
Omim
614652
Umls
C3553358
Sym Map
SMDE02355
Do Class
DOID:0014667DOID:630
Dis Ge Net
C3553358
Umls Sty
T047
Etcm Disease
Coenzyme Q10 Deficiency, Primary, 3
Tcmbank Disease
22600
Itcmdb Generated
ITX-DISEASE-2CA6C1174287

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Page Title
Disease Coenzyme Q10 Deficiency, Primary, 3 Details page
Do Class Name
disease of metabolism; genetic disease
Disease Type
disease
Do Disease Class
genetic disease; disease of metabolism
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Coenzyme Q10 Deficiency, Primary, 3
Global Category
Genetic diseases;Metabolic diseases
Anatomical Category
Nephrological diseases
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome