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Chromosome 1, monosomy 1q32 q42: A rare chromosomal disorder where deletion of a portion of chromosome 1 causes various abnormalities such as fetal or newborn death, facial dysmorphism, short stature, finger defects and various other anomalies. More detailed information about the symptoms, causes, and treatments of Chromosome 1, monosomy 1q32 q42 is available below.
See full list of 24 symptoms of Chromosome 1, monosomy 1q32 q42
Read more about causes of Chromosome 1, monosomy 1q32 q42.
Research the causes of these diseases that are similar to, or related to, Chromosome 1, monosomy 1q32 q42:
See full list of 20 occasional symptoms of Chromosome 1, monosomy 1q32 q42
Types of Chromosome 1, monosomy 1q32 q42
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Chromosome 1, monosomy 1q32 q42 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Chromosome 1, monosomy 1q32 q42, or a subtype of Chromosome 1, monosomy 1q32 q42,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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