DiseaseID 18408

线粒体复合物III缺乏症核基因2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: 1Formula: 21Symptom: 10Target: 18Links: 55
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Record Fields

Scalar fields from the final disease record.

Disease Id
18408
Core Entity Id
76801
Source Entity Count
1
Preferred Name
Mitochondrial Complex Iii Deficiency, Nuclear Type 2
Name Cn
线粒体复合物III缺乏症核基因2型
Name Pinyin
Xian Li Ti Fu He Wu Iii Que Fa Zheng He Ji Yin 2 Xing
Name En
Mitochondrial Complex Iii Deficiency, Nuclear Type 2
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
Mitochondrial Complex Iii Deficiency, Nuclear Type 2
Role
preferred
Name
MC3DN2
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS021878
Omim
615157
Umls
C3554605
Sym Map
SMDE04049
Do Class
DOID:0014667DOID:630
Dis Ge Net
C3554605
Umls Sty
T047
Etcm Disease
Mitochondrial Complex Iii Deficiency, Nuclear Type 2
Tcmbank Disease
13480
Itcmdb Generated
ITX-DISEASE-CEF0382DB31C

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Page Title
Disease Mitochondrial Complex Iii Deficiency, Nuclear Type 2 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
Mitochondrial Complex Iii Deficiency, Nuclear Type 2
Global Category
Genetic diseases;Metabolic diseases
Anatomical Category
Neuronal diseases
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome