Keratoacanthoma familial (medical condition): A rare inherited condition characterized by sebaceous gland tumors on the skin and internal malignancies usually involving the digestive tract.
See also:
Keratoacanthoma, familial:
»Introduction: Keratoacanthoma, familial
»Symptoms of Keratoacanthoma, familial
These medical condition or symptom topics may be relevant to medical information for Keratoacanthoma familial:
Keratoacanthoma familial is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Keratoacanthoma familial, or a subtype of Keratoacanthoma familial,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when if affects 1 person per 2,000.
They list Keratoacanthoma familial as a "rare disease".
Source - Orphanet
Keratoacanthoma familial (medical condition): See Keratoacanthoma, familial (disease information).
»Introduction: Keratoacanthoma, familial
»Symptoms of Keratoacanthoma, familial
These medical disease topics may be related to Keratoacanthoma familial:
Source - NIH
Search to find out more about Keratoacanthoma familial:
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