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X-linked distal spinal muscular atrophy type 3 (disorder)
X-linked distal spinal muscular atrophy type 3
ATP7A (ATPase copper transporting alpha) related distal motor neuropathy
X-linked distal hereditary motor neuropathy type 3
A rare distal hereditary motor neuropathy with characteristics of slowly progressive atrophy and weakness of distal muscles of hands and feet with normal deep tendon reflexes or absent ankle reflexes and minimal or no sensory loss, sometimes mild proximal weakness in the legs and feet and hand deformities in males.
X-gebonden distale spinale spieratrofie type 3
X-gebonden distale spinale musculaire atrofie type 3
X-gebonden distale erfelijke motorische neuropathie type 3
SMAX3
ATP7A-gerelateerde distale motorische neuropathie
X-gebonden distale hereditaire motorische neuropathie type 3
Id766764008
StatusPrimitive
Finding siteNerve structure
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetG12.2
RuleTRUE
AdviceALWAYS G12.2
CorrelationSNOMED CT source code to target map code correlation not specified