DiseaseID 13936

眼咽远端肌病

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: 1Symptom: 1Target: 9Links: 10
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Record Fields

Scalar fields from the final disease record.

Disease Id
13936
Core Entity Id
71649
Source Entity Count
1
Preferred Name
Oculopharyngodistal Myopathy
Name Cn
眼咽远端肌病
Name Pinyin
Yan Yan Yuan Duan Ji Bing
Name En
Oculopharyngodistal Myopathy
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Musculoskeletal Diseases
Do Class
Hpo Class
Mesh Class Name
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
Hpo Class Name
Do Class Name
Disease Definition
Version
v2
Suppressed
No

Names

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

Name
Oculopharyngodistal Myopathy
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS015210
Omim
164310
Umls
C1834014
Sym Map
SMDE11582
Dis Ge Net
C1834014
Umls Sty
T047
Me Sh Class
C05C10C16
Tcmbank Disease
22914

Attributes

Merged source attributes and domain-specific metadata.

Version
v2
Suppress
0
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Musculoskeletal Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
Umls Semantic Type Name
Disease or Syndrome