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SMAX1 (medical condition): A rare condition characterized by progressive...more »
SMAX1 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that SMAX1, or a subtype of SMAX1,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
SMAX1: Another name for Spinal Muscular Atrophy (or close medical condition association).
»Introduction: Spinal Muscular Atrophy
»Symptoms of Spinal Muscular Atrophy
»Treatments for Spinal Muscular Atrophy
SMAX1: SMAX1 is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of SMAX1 incude:
Treatments for SMAX1 (Spinal Muscular Atrophy) include:
Treatment of SMAX1: For more treatment information about SMAX1, see treatment of Spinal Muscular Atrophy (SMAX1)
Death of spinal motor neurons and subsequent muscle paralysis characterize Spinal Muscular Atrophy (SMA), a hereditary neuromuscular...(Source: Genes and Disease by the National Center for Biotechnology)
Spinal muscular atrophy (SMA) is a genetic, motor neuron disease characterized by wasting of the... (Source: excerpt from NINDS Spinal Muscular Atrophy Information Page: NINDS)
These medical disease topics may be related to SMAX1:
Source - NIH
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