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LFS1 (medical condition): A rare inherited disorder characterized by tumor development by young...more »
LFS1 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that LFS1, or a subtype of LFS1,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
LFS1: LFS1 is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of LFS1 incude:
These medical disease topics may be related to LFS1:
Source - NIH
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