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Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Cutaneous mastocytosis as a "rare disease".
Source - Orphanet
Cutaneous mastocytosis: Introduction
Broader types of Cutaneous mastocytosis:
Prevalance of Cutaneous mastocytosis: rare
Prevalance of Cutaneous mastocytosis:
mastocytosis generally
has been considered to be an "orphan disease." (Orphan diseases
affect 200,000 or fewer people in the United States.) (Source: excerpt from Mastocytosis, NIAID Fact Sheet: NIAID)
Symptoms of Cutaneous mastocytosis: see symptoms of Cutaneous mastocytosis
Diagnostic testing: see tests for Cutaneous mastocytosis.
Misdiagnosis: see misdiagnosis and Cutaneous mastocytosis.
Treatments for Cutaneous mastocytosis:
see treatments for Cutaneous mastocytosis
Research for Cutaneous mastocytosis:
see research for Cutaneous mastocytosis
Organs and body systems related to Cutaneous mastocytosis include:
Main name of condition: Cutaneous mastocytosis
Other names or spellings for Cutaneous mastocytosis:urticaria pigmentosa, UP, infantile mastocytosis
Research the causes of these diseases that are similar to, or related to, Cutaneous mastocytosis:
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