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Palatal anomalies, widely spaced teeth, facial dysmorphism, developmental delay syndrome (disorder)
Palatal anomalies, widely spaced teeth, facial dysmorphism, developmental delay syndrome
Palatal anomalies, multiple diastemata, facial dysmorphism, developmental delay syndrome
A rare genetic multiple congenital anomalies/dysmorphic syndrome with characteristics of global developmental delay, axial hypotonia, palate abnormalities (including cleft palate and/or high and narrow palate), dysmorphic facial features (including prominent forehead, hypertelorism, downslanting palpebral fissures, wide nasal bridge, thin lips and widely spaced teeth) and short stature. Additional manifestations may include digital anomalies (such as brachydactyly, clinodactyly and hypoplastic toenails) a single palmar crease, lower limb hypertonia, joint hypermobility along with ocular and urogenital anomalies.
syndroom van afwijking van palatum, grote tussenruimte tussen gebitselementen, faciale dysmorfie en ontwikkelingsachterstand
syndroom van anomalie van verhemelte, grote tussenruimte tussen dentes, faciale dysmorfie en ontwikkelingsachterstand
syndroom van afwijking van gehemelte, grote tussenruimte tussen gebitselementen, faciale dysmorfie en ontwikkelingsachterstand
syndroom van palatinale afwijking, ver uit elkaar staande tanden en/of kiezen, faciale dysmorfie en ontwikkelingsachterstand
Id1172889005
StatusPrimitive
Has interpretationIncreased
InterpretsSpacing of teeth
Associated morphologyMorphologically abnormal structure
Finding siteDentition
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyMorphologically abnormal structure
Finding siteFace structure
OccurrenceCongenital
Pathological processPathological developmental process
ICD-10 complex map reference set
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