| ventriculomegalie en polycysteuze nierziekte (aandoening) | | ventriculomegalie en polycysteuze nierziekte | | syndroom van congenitale nefrose en vergroting van hersenventrikel
ventriculomegalie en cystenieren
| | Cerebral ventriculomegaly, cystic kidney disease | | VMCKD - ventriculomegaly with cystic kidney disease
Congenital nephrosis, cerebral ventriculomegaly syndrome
| | A rare genetic syndrome with a central nervous system malformation as a major feature, and characteristics of a triad of high alpha-fetoprotein levels in both maternal serum and amniotic fluid, cerebral ventriculomegaly, renal macro and microcysts. Variable findings include congenital nephrotic syndrome, aqueductal stenosis, gray matter heterotopias and cardiac malformations among others. |
| | Id | 1216942009 | | Status | Primitive |
| SNOMED CT to Orphanet simple map | 443988 |
| SNOMED CT to ICD-10 extended map | | Target | Q07.8 | | Rule | TRUE | | Advice | ALWAYS Q07.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | | Correlation | SNOMED CT source code to target map code correlation not specified |
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