DiseaseID 21643

常染色体隐性遗传1型伴线粒体DNA缺失的进行性外眼肌麻痹

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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: 1Symptom: 6Target: 2Links: 8
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Record Fields

Scalar fields from the final disease record.

Disease Id
21643
Core Entity Id
80380
Source Entity Count
1
Preferred Name
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Recessive 1
Name Cn
常染色体隐性遗传1型伴线粒体DNA缺失的进行性外眼肌麻痹
Name Pinyin
Chang Ran Se Ti Yin Xing Yi Chuan 1 Xing Ban Xian Li Ti Dna Que Shi De Jin Xing Xing Wai Yan Ji Ma Bi
Name En
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Recessive 1
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
v1
Suppressed
No

Names

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

Name
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Recessive 1
Role
preferred
Name
Autosomal Recessive Progressive External Ophthalmoplegia 1
Role
alias
Name
PEOB1
Role
alias
Name
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE 1
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS025608
Omim
258450
Umls
C4225153
Sym Map
SMDE02295
Do Class
DOID:630DOID:7
Dis Ge Net
C4225153
Umls Sty
T047
Tcmbank Disease
7449

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
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
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome