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Monosomy 1p22 p13 (medical condition): A rare chromosomal disorder where deletion of a portion...more »
These medical condition or symptom topics may be relevant to medical information for Monosomy 1p22 p13:
Monosomy 1p22 p13 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Monosomy 1p22 p13, or a subtype of Monosomy 1p22 p13,
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 Monosomy 1p22 p13 as a "rare disease".
Source - Orphanet
Monosomy 1p22 p13: Another name for Chromosome 1, monosomy 1p22 p13 (or close medical condition association).
»Introduction: Chromosome 1, monosomy 1p22 p13
»Symptoms of Chromosome 1, monosomy 1p22 p13
Monosomy 1p22 p13: Monosomy 1p22 p13 is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of Monosomy 1p22 p13 incude:
These medical disease topics may be related to Monosomy 1p22 p13:
Source - NIH
Search to find out more about Monosomy 1p22 p13:
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