DiseaseID 18331

原发性辅酶Q10缺乏症6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: 2Target: 20Links: 26
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Record Fields

Scalar fields from the final disease record.

Disease Id
18331
Core Entity Id
76713
Source Entity Count
1
Preferred Name
Coenzyme Q10 Deficiency, Primary, 6
Name Cn
原发性辅酶Q10缺乏症6型
Name Pinyin
Yuan Fa Xing Fu Mei Q10 Que Fa Zheng 6 Xing
Name En
Coenzyme Q10 Deficiency, Primary, 6
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, 6
Role
preferred
Name
COQ10D6
Role
alias
Name
Primary Coenzyme Q10 Deficiency 6
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS021748
Omim
614650
Umls
C3553349
Sym Map
SMDE03362
Do Class
DOID:0014667DOID:630
Dis Ge Net
C3553349
Umls Sty
T047
Etcm Disease
Coenzyme Q10 Deficiency, Primary, 6
Tcmbank Disease
3008
Itcmdb Generated
ITX-DISEASE-96BC13CFEC56

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Page Title
Disease Coenzyme Q10 Deficiency, Primary, 6 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, 6
Global Category
Fetal diseases;Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Ear diseases;Nephrological diseases;Neuronal diseases
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome