Autosomal dominant hereditary disorder
Constitutional aplastic anemia
Developmental hereditary disorder
Hereditary white blood cell disorder
Inherited platelet disorder
Multiple malformation syndrome with limb defect as major feature
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WT limb blood syndrome (disorder)
WT limb blood syndrome
Syndrome is characterized by hematological anomalies (Fanconi anemia, leukemia and lymphoma) often appearing during childhood. Anomalies of the limbs and hands are also present: bifid or hypoplastic thumbs, cutaneous syndactyly and ulnar and radial defects. The syndrome has been described in several families. Transmission is autosomal dominant.
WT-bloedsyndroom van extremiteit
WT-bloedsyndroom van ledemaat
Id719019000
StatusPrimitive
Associated morphologyAplasia
Finding siteBone marrow structure
OccurrenceCongenital
Pathological processPathological developmental process
Has interpretationBelow reference range
InterpretsWhite blood cell count
Has interpretationBelow reference range
InterpretsRed blood cell count
Has interpretationBelow reference range
InterpretsPlatelet count
Has interpretationBelow reference range
InterpretsMeasurement of total hemoglobin concentration
Due toDecreased erythrocyte production
Pathological processAbnormal immune process
Has interpretationAbnormal
InterpretsHemostatic function
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetD61.0
RuleTRUE
AdviceALWAYS D61.0 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified