Autosomal recessive hereditary disorder
Cleft palate with cleft lip
Congenital anomaly of face bones
Developmental hereditary disorder
Digestive system hereditary disorder
Hereditary disorder of musculoskeletal system
Hereditary nephropathy
Multiple system malformation syndrome
Potter's facies
Renal agenesis
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Holzgreve syndrome (disorder)
Holzgreve syndrome
Cleft palate, Potter sequence, congenital heart anomalies, mesoaxial polydactyly, multiple malformations syndrome
Holzgreve Wagner Rehder syndrome
An extremely rare lethal multiple congenital anomalies/dysmorphic syndrome with characteristics of renal agenesis with Potter sequence, cleft lip/palate, oral synechiae, cardiac defects, and skeletal abnormalities including postaxial polydactyly. Intestinal nonfixation and intrauterine growth restriction are also associated. There have been no further descriptions in the literature since 1988.
syndroom van palatoschisis, Potter-sequentie, congenitale hartafwijking, mesoaxiale polydactylie en multipele malformaties
syndroom van Holzgreve
Holzgreve-syndroom
Id783159001
StatusPrimitive
Associated morphologyMorphologically abnormal structure
Finding siteBone structure of face
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyDevelopmental failure of fusion
Finding siteLip structure
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyAgenesis
Finding siteEntire kidney
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyDevelopmental failure of fusion
Finding sitePalatal structure
OccurrenceCongenital
Pathological processPathological developmental process
Due toOligohydramnios
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