All diseases

OMIM ID
301830
OMIM term:
SPINAL MUSCULAR ATROPHY, X-LINKED 2; SMAX2
Alternative terms:
SPINAL MUSCULAR ATROPHY, X-LINKED LETHAL INFANTILE
SPINAL MUSCULAR ATROPHY, INFANTILE X-LINKED; XLSMA
ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, X-LINKED
AMC, DISTAL, X-LINKED
ARTHROGRYPOSIS, X-LINKED, TYPE I; AMCX1
(∗) Location:
Xp11.23  
(†) Associated OMIM genes:
UBA1  
(‡) Associated MGI genes:

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