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Monosomy 10pter (medical condition): A very rare syndrome caused by a chromosomal defect (10p...more »
These medical condition or symptom topics may be relevant to medical information for Monosomy 10pter:
Monosomy 10pter is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Monosomy 10pter, or a subtype of Monosomy 10pter,
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 10pter as a "rare disease".
Source - Orphanet
Monosomy 10pter: Another name for Chromosome 10p terminal deletion syndrome (or close medical condition association).
»Introduction: Chromosome 10p terminal deletion syndrome
»Symptoms of Chromosome 10p terminal deletion syndrome
Monosomy 10pter: Monosomy 10pter is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of Monosomy 10pter incude:
Source - NIH
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