Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Formula: 20Symptom: 7Target: 16Links: 51
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 16046
- Core Entity Id
- 74063
- Source Entity Count
- 1
- Preferred Name
- Combined Oxidative Phosphorylation Deficiency 3
- Name Cn
- 联合氧化磷酸化缺陷3型
- Name Pinyin
- Lian He Yang Hua Lin Suan Hua Que Xian 3 Xing
- Name En
- Combined Oxidative Phosphorylation Deficiency 3
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Musculoskeletal Diseases; Nervous System Diseases; Nutritional and Metabolic Diseases; Pathological Conditions, Signs and Symptoms
- Do Class
- genetic disease; disease of metabolism
- Hpo Class
- Mesh Class Name
- Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases
- 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
Combined Oxidative Phosphorylation Deficiency 3
Role
preferred
Name
CONCENTRIC CARDIOMYOPATHY, HYPOTONIA, AND LACTIC ACIDOSIS
Role
alias
Name
COXPD3
Role
alias
Name
ENCEPHALOMYOPATHY, RESPIRATORY FAILURE, AND LACTIC ACIDOSIS
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS018132
Omim
610505
Umls
C1864840
Sym Map
SMDE02025
Do Class
DOID:0014667DOID:630
Dis Ge Net
C1864840
Umls Sty
T047
Me Sh Class
C05C10C18C23
Etcm Disease
Combined Oxidative Phosphorylation Deficiency 3
Tcmbank Disease
26425
Itcmdb Generated
ITX-DISEASE-03C0AE09D82A
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Page Title
Disease Combined Oxidative Phosphorylation Deficiency 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
Combined Oxidative Phosphorylation Deficiency 3
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Cardiovascular diseases
Me Sh Disease Class
Musculoskeletal Diseases; Nervous System Diseases; Nutritional and Metabolic Diseases; Pathological Conditions, Signs and Symptoms
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases
Umls Semantic Type Name
Disease or Syndrome