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syndroom van hypopituïtarisme door lege sella turcica (aandoening)
syndroom van hypopituïtarisme door lege sella turcica
syndroom van hypofysedeficiëntie als gevolg van lege sella turcica
Pituitary deficiency due to empty sella turcica syndrome
Hypopituitarism due to empty sella turcica syndrome
A rare pituitary deficiency characterized by herniation of the subarachnoid space into the sella turcica, resulting in flattening of the pituitary gland and endocrine dysfunction. Most common endocrine abnormalities are hyperprolactinemia and growth hormone deficit. Clinical symptoms are highly variable and include headaches, irregular menstruation, galactorrhea, obesity, and visual disturbances, among others.
Id715668008
StatusPrimitive
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetE23.0
TermHypopituïtarisme
SNOMED CT to Orphanet simple map91354
SNOMED CT to ICD-10 extended map
TargetE23.0
RuleTRUE
AdviceALWAYS E23.0 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified