DiseaseID 26424

弥漫性皮肤型系统性硬化症

Diffuse Cutaneous Systemic Sclerosis

Diffuse cutaneous systemic sclerosis (dcSSc) is a subtype of Systemic Sclerosis (SSc; see this term) characterized by truncal and acral skin fibrosis with an early and significant incidence of diffuse

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: 1Formula: 1Herb: 3Symptom: 7Target: 17Links: 35
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
26424
Core Entity Id
118992
Source Entity Count
1
Preferred Name
Diffuse Cutaneous Systemic Sclerosis
Name Cn
弥漫性皮肤型系统性硬化症
Name Pinyin
Mi Man Xing Pi Fu Xing Xi Tong Xing Ying Hua Zheng
Name En
Diffuse Cutaneous Systemic Sclerosis
Name Latin
Bilingual Status
complete
Disease Type
Umls Disease Type
Disgenet Type
Mesh Class
Do Class
Hpo Class
Mesh Class Name
Hpo Class Name
Do Class Name
Disease Definition
Diffuse cutaneous systemic sclerosis (dcSSc) is a subtype of Systemic Sclerosis (SSc; see this term) characterized by truncal and acral skin fibrosis with an early and significant incidence of diffuse
Version
v1
Suppressed
No

Names

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

Name
Diffuse Cutaneous Systemic Sclerosis
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Sym Map
SMDE03399
Orphanet
220393
Etcm Disease
Diffuse Cutaneous Systemic Sclerosis
Itcmdb Generated
ITX-DISEASE-E56F7F003B40

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
Suppress
0
Page Title
Disease Diffuse Cutaneous Systemic Sclerosis Details page
Basic Information
Disease Name
Diffuse Cutaneous Systemic Sclerosis
Global Category
Rare diseases
Anatomical Category
Bone diseases;Nephrological diseases;Respiratory diseases;Skin diseases
Disease Definition
Diffuse cutaneous systemic sclerosis (dcSSc) is a subtype of Systemic Sclerosis (SSc; see this term) characterized by truncal and acral skin fibrosis with an early and significant incidence of diffuse