All diseases

OMIM ID
158600
OMIM term:
SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY, AUTOSOMAL DOMINANT; SMALED
Alternative terms:
SMA-LED
SPINAL MUSCULAR ATROPHY, CHILDHOOD, PROXIMAL, AUTOSOMAL DOMINANT
SPINAL MUSCULAR ATROPHY, JUVENILE, PROXIMAL, AUTOSOMAL DOMINANT
KUGELBERG-WELANDER SYNDROME, AUTOSOMAL DOMINANT
(∗) Location:
14q32   14q32.31  
(†) Associated OMIM genes:
DYNC1H1  
(‡) Associated MGI genes:

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