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Fatty acyl-coenzyme A reductase 1 deficiency (disorder)
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 characterized by syndromic severe intellectual disability with congenital cataracts, early-onset epilepsy, microcephaly, global developmental delay, growth retardation and 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
Finding siteCerebrum
Has interpretationImpaired
InterpretsIntellectual ability
Has interpretationImpaired
InterpretsAdaptation behavior
Has interpretationBelow reference range
InterpretsBody height
Has interpretationBelow reference range
InterpretsHead circumference
SNOMED CT to Orphanet simple map
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