Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
Click a node to open it in a new tab
Disease: 1Symptom: 10Target: 1Links: 11
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 16033
- Core Entity Id
- 74048
- Source Entity Count
- 1
- Preferred Name
- Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 4
- Name Cn
- 常染色体显性进行性眼外肌麻痹伴线粒体DNA缺失4型
- Name Pinyin
- Chang Ran Se Ti Xian Xing Jin Xing Xing Yan Wai Ji Ma Bi Ban Xian Li Ti Dna Que Shi 4 Xing
- Name En
- Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 4
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Nervous System Diseases; Nutritional and Metabolic Diseases; Eye Diseases; Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
- Do Class
- disease of anatomical entity; genetic disease
- Hpo Class
- Mesh Class Name
- Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Eye Diseases; Musculoskeletal Diseases; Nervous System Diseases
- Hpo Class Name
- Do Class Name
- genetic disease; disease of anatomical entity
- Disease Definition
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 4
Role
preferred
Name
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant 4
Role
preferred
Name
Autosomal Dominant Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions 4
Role
alias
Name
PEOA4
Role
alias
Name
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL DOMINANT 4
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS018110
Omim
610131
Umls
C1864668
Sym Map
SMDE03310
Do Class
DOID:630DOID:7
Dis Ge Net
C1864668
Umls Sty
T047
Me Sh Class
C05C10C11C18C23
Tcmbank Disease
31005
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Do Class Name
genetic disease; disease of anatomical entity
Disease Type
disease
Do Disease Class
disease of anatomical entity; genetic disease
Umls Disease Type
Disease or Syndrome
Me Sh Disease Class
Nervous System Diseases; Nutritional and Metabolic Diseases; Eye Diseases; Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Eye Diseases; Musculoskeletal Diseases; Nervous System Diseases
Umls Semantic Type Name
Disease or Syndrome