Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Target: 19Links: 24
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 1506
- Core Entity Id
- 1696
- Source Entity Count
- 1
- Preferred Name
- Mitochondrial Complex I Deficiency, Nuclear Type 20
- Name Cn
- 线粒体复合物I缺乏症，核型20
- Name Pinyin
- Xian Li Ti Fu He Wu I Que Fa Zheng ， He Xing 20
- Name En
- Mitochondrial Complex I Deficiency, Nuclear Type 20
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Nutritional and Metabolic Diseases; Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
- Do Class
- Hpo Class
- Mesh Class Name
- Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases
- Hpo Class Name
- Do Class Name
- Disease Definition
- Version
- Suppressed
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Mitochondrial Complex I Deficiency, Nuclear Type 20
Role
preferred
Name
Acyl-CoA Dehydrogenase Family, Member 9, Deficiency of
Role
preferred
Name
Acyl-Coa Dehydrogenase 9 Deficiency
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS018809HBDIS028013
Omim
611126
Dis Ge Net
C1970173C4747517
Umls Sty
T047
Me Sh Class
C05C10C14C16C18C23
Etcm Disease
Mitochondrial Complex I Deficiency, Nuclear Type 20
Tcmbank Disease
1877027404
Itcmdb Generated
ITX-DISEASE-5C031F771711
Attributes
Merged source attributes and domain-specific metadata.
Page Title
Disease Mitochondrial Complex I Deficiency, Nuclear Type 20 Details page
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Mitochondrial Complex I Deficiency, Nuclear Type 20
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Cardiovascular diseases;Liver diseases;Neuronal diseases
Me Sh Disease Class
Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Nutritional and Metabolic Diseases; Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases
Umls Semantic Type Name
Disease or Syndrome