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Diseases

Localized scleroderma

localized 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
Localized scleroderma
Standard Disease Name
localized scleroderma
MeSH Tree
No data
ICD-10
L94.0

Identifiers

DO ID
No data
MeSH ID
D012594
OMIM ID
No data
UMLS ID
C0036420
HPO ID
No data

Description and Extensions

Description
NCI2016_NICHD_1602D:An autoimmune disorder marked by excessive production of collagen resulting in hardening and thickening of skin, with formation of patches or lines of thick and unyielding tissue. There can also be musculoskeletal and underlying tissue involvement. The affected areas of skin can be restrictive and disfiguring.|NCI2016_02D:A chronic disorder, possibly autoimmune, marked by excessive production of collagen which results in hardening and thickening of body tissues. Localized scleroderma typically affects the skin, with formation of patches or lines of thick and unyielding tissue; there can be muscle and underlying tissue involvement as well as occasional joint complications. The affected areas of skin can be restrictive and disfiguring. The shape, depth and location of the affected area is used to classify one of the four types of local scleroderma. An individual can have a combination of localized scleroderma types.|MSH2017_2016_08_12:A term used to describe a variety of localized asymmetrical SKIN thickening that is similar to those of SYSTEMIC SCLERODERMA but without the disease features in the multiple internal organs and BLOOD VESSELS. Lesions may be characterized as patches or plaques (morphea), bands (linear), or nodules.
Related

Direct relations and traceable candidates grouped by relation type.

Candidate Herbs

target disease -> ingredient target -> herb ingredient8 Herbs