DiseaseID 12119
弥漫性硬皮病
disease
NCI2016_NICHD_1602D:A variant of systemic scleroderma characterized by sclerosis of the skin, Raynaud phenomenon, and organ involvement, including pulmonary fibrosis, renal disease, and gastrointestinal tract involvement
Relationship Network
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Disease: 1Symptom: 12Target: 12Links: 24
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 12119
- Core Entity Id
- 69594
- Source Entity Count
- 1
- Preferred Name
- Diffuse Scleroderma
- Name Cn
- 弥漫性硬皮病
- Name Pinyin
- Mi Man Xing Ying Pi Bing
- Name En
- Diffuse Scleroderma
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Skin and Connective Tissue Diseases
- Do Class
- disease of anatomical entity
- Hpo Class
- Mesh Class Name
- Skin and Connective Tissue Diseases
- Hpo Class Name
- Do Class Name
- disease of anatomical entity
- Disease Definition
- NCI2016_NICHD_1602D:A variant of systemic scleroderma characterized by sclerosis of the skin, Raynaud phenomenon, and organ involvement, including pulmonary fibrosis, renal disease, and gastrointestinal tract involvement.|NCI2016_02D:A variant of systemic scleroderma characterized by sclerosis of the skin, Raynaud phenomenon, and organ involvement, including pulmonary fibrosis, renal disease, and gastrointestinal tract involvement.|MSH2017_2016_08_12:A rapid onset form of SYSTEMIC SCLERODERMA with progressive widespread SKIN thickening over the arms, the legs and the trunk, resulting in stiffness and disability.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Diffuse Scleroderma
Role
preferred
Name
Scleroderma, Diffuse
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS012826
Me Sh
D045743
Umls
C1258104
Sym Map
SMDE07914
Do Class
DOID:7
Dis Ge Net
C1258104
Umls Sty
T047
Me Sh Class
C17
Tcmbank Disease
30747
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Do Class Name
disease of anatomical entity
Disease Type
disease
Do Disease Class
disease of anatomical entity
Umls Disease Type
Disease or Syndrome
Disease Definition
NCI2016_NICHD_1602D:A variant of systemic scleroderma characterized by sclerosis of the skin, Raynaud phenomenon, and organ involvement, including pulmonary fibrosis, renal disease, and gastrointestinal tract involvement.|NCI2016_02D:A variant of systemic scleroderma characterized by sclerosis of the skin, Raynaud phenomenon, and organ involvement, including pulmonary fibrosis, renal disease, and gastrointestinal tract involvement.|MSH2017_2016_08_12:A rapid onset form of SYSTEMIC SCLERODERMA with progressive widespread SKIN thickening over the arms, the legs and the trunk, resulting in stiffness and disability.
Me Sh Disease Class
Skin and Connective Tissue Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Skin and Connective Tissue Diseases
Umls Semantic Type Name
Disease or Syndrome