|||||||
XY type gonadal dysgenesis with associated anomalies syndrome (disorder)
XY type gonadal dysgenesis with associated anomalies syndrome
Gonadal dysgenesis XY type with associated anomalies
An association syndrome described only once in two sisters. They had a 46,XY karyotype, cleft lip and palate, preauricular pits and a 'squashed down' appearance because of a short columella and small nares. Other anomalies included broad hands and feet, and a hypermuscular appearance. Cardiac, renal, musculoskeletal and ectodermal anomalies were also present. Ectodermal defects included 'punched out scalp defects' and unusual positioning of hair whorls. They also had short stature, streak gonads, and mild developmental delay.
syndroom van gonadale dysgenesie type XY met geassocieerde anomalieën
gonadale dysgenesie type XY met geassocieerde anomalieën-syndroom
Id733605002
StatusPrimitive
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
TargetQ99.1
RuleTRUE
AdviceALWAYS Q99.1 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified