Duplication 3q13.2 q25 (medical condition): A rare chromosomal disorder characterized by various abnormalities including hearing loss, mental retardation, short stature, obesity and uterine and facial anomalies.
See also:
Chromosome 3, trisomy 3q13 2 q25:
»Introduction: Chromosome 3, trisomy 3q13 2 q25
»Symptoms of Chromosome 3, trisomy 3q13 2 q25
These medical condition or symptom topics may be relevant to medical information for Duplication 3q13.2 q25:
Duplication 3q13.2 q25 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Duplication 3q13.2 q25, or a subtype of Duplication 3q13.2 q25,
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 Duplication 3q13.2 q25 as a "rare disease".
Source - Orphanet
Duplication 3q13.2 q25: Another name for Chromosome 3, trisomy 3q13 2 q25 (or close medical condition association).
»Introduction: Chromosome 3, trisomy 3q13 2 q25
»Symptoms of Chromosome 3, trisomy 3q13 2 q25
Some of the symptoms of Duplication 3q13.2 q25 incude:
See full list of 20 symptoms of Duplication 3q13.2 q25 (Chromosome 3, trisomy 3q13 2 q25)
Source - NIH
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