DiseaseID 17515

常染色体显性遗传包涵体肌病

disease

Back to Browse

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: 1Target: 12Links: 13
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
17515
Core Entity Id
75760
Source Entity Count
1
Preferred Name
Inclusion Body Myopathy, Autosomal Dominant
Name Cn
常染色体显性遗传包涵体肌病
Name Pinyin
Chang Ran Se Ti Xian Xing Yi Chuan Bao Han Ti Ji Bing
Name En
Inclusion Body Myopathy, Autosomal Dominant
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Musculoskeletal Diseases; Eye Diseases; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Do Class
Hpo Class
Mesh Class Name
Pathological Conditions, Signs and Symptoms; Eye Diseases; 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
Inclusion Body Myopathy, Autosomal Dominant
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS020358
Umls
C2931820
Sym Map
SMDE09811
Dis Ge Net
C2931820
Umls Sty
T047
Me Sh Class
C05C10C11C23
Tcmbank Disease
7546

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
Musculoskeletal Diseases; Eye Diseases; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Pathological Conditions, Signs and Symptoms; Eye Diseases; Musculoskeletal Diseases; Nervous System Diseases
Umls Semantic Type Name
Disease or Syndrome