DiseaseID 1537

常染色体隐性遗传性进行性外眼肌麻痹伴线粒体DNA缺失5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: 1Target: 1Links: 1
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
1537
Core Entity Id
1731
Source Entity Count
1
Preferred Name
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Recessive 5
Name Cn
常染色体隐性遗传性进行性外眼肌麻痹伴线粒体DNA缺失5型
Name Pinyin
Chang Ran Se Ti Yin Xing Yi Chuan Xing Jin Xing Xing Wai Yan Ji Ma Bi Ban Xian Li Ti Dna Que Shi 5 Xing
Name En
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Recessive 5
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Do Class
disease of anatomical entity; genetic disease
Hpo Class
Mesh Class Name
Hpo Class Name
Do Class Name
genetic disease; disease of anatomical entity
Disease Definition
Version
Suppressed

Names

Preferred names, aliases, and source labels retained in the final schema.

Name
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Recessive 5
Role
preferred
Name
Autosomal Recessive Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions 5
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS028045
Omim
618098
Do Class
DOID:630DOID:7
Dis Ge Net
C4748184
Umls Sty
T047
Tcmbank Disease
3800

Attributes

Merged source attributes and domain-specific metadata.

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
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome