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'WW domain containing adaptor with coiled-coil'-gerelateerd syndroom van faciale dysmorfie, ontwikkelingsachterstand en gedragsstoornis (aandoening)
WAC-gerelateerd syndroom van faciale dysmorfie, ontwikkelingsachterstand en gedragsstoornis
'WW domain containing adaptor with coiled-coil'-gerelateerd syndroom van faciale dysmorfie, ontwikkelingsachterstand en gedragsstoornis
WAC-related facial dysmorphism, developmental delay, behavioral abnormalities syndrome
WW domain containing adaptor with coiled-coil-related facial dysmorphism, developmental delay, behavioral abnormalities syndrome
A rare genetic syndromic intellectual disability characterized by several dysmorphic features, hypotonia, developmental delay, intellectual disability, behavioral problems, visual and hearing abnormalities, constipation, and feeding difficulties. Common dysmorphic features include coarse facies, broad forehead, synophrys, bushy eyebrows, deep-set eyes, downslanting palpebral fissures, epicanthus, depressed nasal bridge, bulbous nasal tip, posteriorly rotated ears, full cheeks, thin upper lip, inverted nipples and hirsutism. Behavioral problems tend to be dominated by attention deficit hyperactivity disorder, but anxiety, aggressive outbursts and autistic features may also present.
Id1187247007
StatusPrimitive
Has interpretationgestoord
Interpretsintellectueel vermogen
Has interpretationgestoord
InterpretsAdaptation behavior
SNOMED CT to Orphanet simple map466943
SNOMED CT to ICD-10 extended map
TargetQ87.0
RuleTRUE
AdviceALWAYS Q87.0 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified
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