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Fallot complex with intellectual disability and growth delay syndrome (disorder)
Fallot complex with intellectual disability and growth delay syndrome
Bindewald Ulmer Muller syndrome
A rare disorder characterized by tetralogy of Fallot, minor facial anomalies, and severe intellectual deficiency and growth delay. Dysmorphic features include large, protruding, abnormally modeled ears and broad nasal root. Microcephaly and syndactyly of second and third toes have also been recorded. All patients have severe intellectual deficiency. The condition is transmitted as an autosomal recessive trait.
syndroom van tetralogie van Fallot, verstandelijke beperking en groeiachterstand
syndroom van Bindewald-Ulmer-Müller
syndroom van tetralogie van Fallot, mentale retardatie en groeiachterstand
Id723336008
StatusPrimitive
Associated morphologyHypertrophy
Finding siteEntire right cardiac ventricle
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyOverriding structures
Finding siteThoracic aorta structure
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyStenosis
Finding sitePulmonary valve structure
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyGrowth retardation
Pathological processPathological developmental process
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetQ87.8
RuleTRUE
AdviceALWAYS Q87.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified