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RCDP1 (medical condition): A group of inherited disorder affecting the skeleton,...more »
RCDP1 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that RCDP1, or a subtype of RCDP1,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
RCDP1: RCDP1 is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of RCDP1 incude:
Source - NIH
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