||
maternale riboflavinedeficiëntie (aandoening)
vitamine B2-tekort bij moeder
maternale lactoflavinedeficiëntie
maternale riboflavinedeficiëntie
Maternal riboflavin deficiency
A rare genetic disorder of metabolite absorption or transport with characteristics of persistently decreased riboflavin serum levels due to a primary genetic defect in the mother and which leads to clinical and biochemical findings consistent with a secondary, life-threatening, transient multiple acyl-CoA dehydrogenase deficiency (MADD) in the newborn. The mother usually presents hyperemesis gravidarum in the absence of other features of riboflavin deficiency, such as skin lesions, jaundice, pruritus, sore mucous membranes, visual disturbances.
Id773549000
StatusPrimitive
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetP00.4
TermGevolgen voor foetus en pasgeborene door voedingsstoornissen van moeder
SNOMED CT to Orphanet simple map411712
SNOMED CT to ICD-10 extended map
TargetP00.4
RuleTRUE
AdviceALWAYS P00.4 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified