stoornis van peroxisomale functie
X-gebonden hereditaire aandoening
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ATP binding cassette subfamily D member 1 gene related disorder of peroxisomal function (disorder)
ABCD1 gene related disorder of peroxisomal function
ATP binding cassette subfamily D member 1 gene related disorder of peroxisomal function
Id1407000006
StatusDefined
Occurrencecongenitaal
Has associated geneABCD1 gene
SNOMED CT to ICD-10 extended map
TargetE88.8
RuleTRUE
AdviceALWAYS E88.8
CorrelationSNOMED CT source code to target map code correlation not specified
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'contiguous' ABCD1-DXS1357E-deletiesyndroom
adrenoleukodystrofie4