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Diseases

Diffuse Scleroderma

diffuse scleroderma

Entity Type
Diseases
Relation Groups
3
Relation Preview
24

Basic Information

Grouped by core information, identifiers, and descriptions.

Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.

Core Information

Disease Name
Diffuse Scleroderma
Standard Disease Name
diffuse scleroderma
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
D045743
OMIM ID
No data
UMLS ID
C1258104
HPO ID
No data

Description and Extensions

Description
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.
Related

Direct relations and traceable candidates grouped by relation type.

Candidate Herbs

target disease -> ingredient target -> herb ingredient8 Herbs