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Hydrocephalus with obesity and hypogonadism syndrome (disorder)
Hydrocephalus with obesity and hypogonadism syndrome
Sengers Hamel Otten syndrome
Syndrome with the association of congenital hydrocephalus, centripetal obesity, hypogonadism, intellectual deficit and short stature. It has been described in two males from one family. An X-linked recessive mode of inheritance was suggested.
syndroom van hydrocefalie met obesitas en hypogonadisme
hydrocefalie-obesitas-hypogonadisme-syndroom
hydrocephalus-obesitas-hypogonadisme-syndroom
syndroom van Sengers-Hamel-Otten
Id721231007
StatusPrimitive
Has interpretationAbove reference range
InterpretsBody weight measure
Associated morphologyDilatation
Finding siteBrain cerebrospinal fluid pathway
OccurrenceCongenital
Pathological processPathological developmental process
ICD-10 complex map reference set
TargetQ03.9
RuleTRUE
AdviceALWAYS Q03.9
CorrelationSNOMED CT source code to target map code correlation not specified
TargetE66.8
RuleTRUE
AdviceALWAYS E66.8
CorrelationSNOMED CT source code to target map code correlation not specified
TargetE28.3
RuleIFA 248152002 | Female (finding) |
AdviceIF FEMALE CHOOSE E28.3 | MAP IS CONTEXT DEPENDENT FOR GENDER
CorrelationSNOMED CT source code to target map code correlation not specified
TargetE29.1
RuleIFA 248153007 | Male (finding) |
AdviceIF MALE CHOOSE E29.1 | MAP IS CONTEXT DEPENDENT FOR GENDER
CorrelationSNOMED CT source code to target map code correlation not specified
Target
RuleOTHERWISE TRUE
AdviceMAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA
CorrelationSNOMED CT source code to target map code correlation not specified