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Cholestasis with pigmentary retinopathy and cleft palate syndrome (disorder)
Cholestasis with pigmentary retinopathy and cleft palate syndrome
Hardikar syndrome
A syndrome of multiple congenital malformations with an association of cleft lip and palate, patchy pigmentary retinopathy (cat's paw), obstructive liver disease (cholestasis, portal hypertension) and obstructive renal disease (ectopic ureteric insertion, obstruction, hydronephrosis). Gastrointestinal tract and cardiac involvement have also been reported. An overlap with Kabuki syndrome is debated.
syndroom van cholestase met pigmentretinopathie en palatoschisis
syndroom van Hardikar
syndroom van galstuwing met pigmentretinopathie en gespleten gehemelte
Hardikar-syndroom
Id720636001
StatusPrimitive
Associated morphologyMorphologically abnormal structure
Finding siteLiver structure
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyPigment deposition
Finding siteRetinal structure
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyDevelopmental failure of fusion
Finding siteLip structure
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyDevelopmental failure of fusion
Finding sitePalatal structure
OccurrenceCongenital
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