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'split spinal cord'-malformatie type I (aandoening)
'split spinal cord'-malformatie type I
congenitale myeloschisis type 1
aangeboren gespleten ruggenmerg type I
Split spinal cord malformation type I
Split spinal cord malformation type 1
A rare, neural tube defect characterized by localized longitudinal division of the spinal cord with an interposed osseous, cartilaginous or fibrous septum and double dural sac, typically occurring at the thoracic or lumbar level. Local vertebral segmental defects, syringomyelia, meningocele and intraspinal tumors may be associated. Variable clinical presentation includes pain, scoliosis, asymmetry and weakness of the lower limbs, neurological deficits, sphincter dysfunction, and various cutaneous abnormalities overlying the spine, such as hypertrichosis, dimple, hemangioma, subcutaneous mass or pigmented nevus.
Id1162826002
StatusPrimitive
Associated morphologyfusiedefect
Finding sitestructuur van arcus vertebrae
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
SNOMED CT to Orphanet simple map1671
SNOMED CT to ICD-10 extended map
TargetQ06.2
RuleTRUE
AdviceALWAYS Q06.2 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified