DiseaseID 15059

常染色体隐性遗传性肌硬化症

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: 2Target: 1Links: 3
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
15059
Core Entity Id
72939
Source Entity Count
1
Preferred Name
Myosclerosis, Autosomal Recessive
Name Cn
常染色体隐性遗传性肌硬化症
Name Pinyin
Chang Ran Se Ti Yin Xing Yi Chuan Xing Ji Ying Hua Zheng
Name En
Myosclerosis, Autosomal Recessive
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Nervous System Diseases; Musculoskeletal Diseases
Do Class
Hpo Class
Mesh Class Name
Musculoskeletal Diseases; Nervous System Diseases
Hpo Class Name
Do Class Name
Disease Definition
Version
v1,v2
Suppressed
No

Names

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

Name
Myosclerosis, Autosomal Recessive
Role
preferred
Name
MYOPATHY, MYOSCLEROTIC
Role
alias
Name
MYOSCLEROSIS, CONGENITAL, OF LOWENTHAL
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS016744
Omim
255600
Umls
C1850671
Sym Map
SMDE00557
Dis Ge Net
C1850671
Umls Sty
T047
Me Sh Class
C05C10
Tcmbank Disease
29710

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Me Sh Disease Class
Nervous System Diseases; Musculoskeletal Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Musculoskeletal Diseases; Nervous System Diseases
Umls Semantic Type Name
Disease or Syndrome