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'chromodomain helicase DNA-binding protein 8'-overgroeisyndroom (aandoening)
CHD8-gerelateerd overgroeisyndroom
'chromodomain helicase DNA-binding protein 8'-overgroeisyndroom
CHD8 overgrowth syndrome
Chromodomain helicase DNA binding protein 8 overgrowth syndrome
CHD8-related intellectual disability, autism, macrocephaly, tall stature syndrome
A rare multiple congenital anomalies/dysmorphic syndrome with characteristics of mild to moderate intellectual disability, autism spectrum phenotype, macrocephaly, tall stature, gastrointestinal problems (including recurrent constipation), distinctive facial features (including wide-set eyes with down-slanted palpebral fissure, broad nose with full nasal tip, pointed chin and broad forehead with prominent supraorbital ridge) and sleep problems. Other clinical manifestations include anxiety problems, attention problems, impaired social interactions, and seizures.
Id1304276001
StatusPrimitive
Associated morphologymorfologische afwijking
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
SNOMED CT to ICD-10 extended map
TargetQ87.3
RuleTRUE
AdviceALWAYS Q87.3 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified