Hereditary cancer-predisposing syndrome
Hereditary disorder of endocrine system
Polyglandular activity in multiple endocrine adenomatosis
|||
Multiple endocrine neoplasia, type 2 (disorder)
Multiple endocrine neoplasia, type 2
PTC syndrome
Sipple syndrome
MEN, type 2
Multiple endocrine adenomatosis, type 2
Familial chromaffinomatosis
Sipple's syndrome
MEA, type 2
multipele endocriene neoplasie type 2
MEN type 2
MEN-2-syndroom
MEN type 2
Multipele endocriene neoplasie syndroom type 2; zeldzame erfelijke ziekte waarbij in diverse klieren en organen gezwellen ontstaan, met name in de schildklier, bijschildklieren en de bijnieren.
Id61808009
StatusPrimitive
Associated morphologyMultiple endocrine adenomas
Finding siteStructure of multiple endocrine glands
PALGA thesaurus simple reference set for pathology
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetD44.8
RuleTRUE
AdviceALWAYS D44.8 | POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE
CorrelationSNOMED CT source code to target map code correlation not specified
|
Benign multiple endocrine neoplasia type 2a
Malignant multiple endocrine neoplasia type 2a
Multiple endocrine neoplasia type 2A