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deficiëntie van vetzuur-acyl-co-enzym-A-reductase 1 (aandoening)
deficiëntie van vetzuur-acyl-co-enzym-A-reductase 1
FAR1-deficiëntie
PFCRD
stoornis van peroxisomaal vetzuur-acyl-CoA-reductase 1
deficiëntie van acyl-CoA-reductase
Fatty acyl-CoA reductase 1 deficiency
FAR1 deficiency
PFCRD - peroxisomal fatty acyl-CoA reductase 1 disorder
Fatty acyl-coenzyme A reductase 1 deficiency
A rare disorder of plasmalogen biosynthesis with characteristics of syndromic severe intellectual disability with congenital cataracts, early-onset epilepsy, microcephaly, global developmental delay, growth retardation, short stature and spastic quadriparesis. Dysmorphic facial features may be present, including high-arched eyebrows, flattened nasal root, hypertelorism and long and smooth philtrum. Rhizomelia is not part of the syndrome. Cerebellar atrophy, white matter abnormalities and Dandy-Walker malformation have been described on brain imaging.
Id1237619001
StatusPrimitive
Associated morphologymorfologische afwijking
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Has interpretationgestoord
Interpretsintellectueel vermogen
Has interpretationgestoord
InterpretsAdaptation behavior
Has interpretationonder referentiebereik
Interpretshoofdomtrek
SNOMED CT to Orphanet simple map438178
SNOMED CT to ICD-10 extended map
TargetE71.3
RuleTRUE
AdviceALWAYS E71.3 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified