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Search 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:
Mouse
Zebrafish
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