Autosomal dominant hereditary disorder
Connective tissue hereditary disorder
Familial partial lipodystrophy
Hereditary disorder of endocrine system
Hereditary disorder of the integument
|||||
AKT serine/threonine kinase 2-related familial partial lipodystrophy (disorder)
AKT2-related familial partial lipodystrophy
AKT serine/threonine kinase 2-related familial partial lipodystrophy
A rare familial partial lipodystrophy with characteristics of adult onset of distal lipoatrophy and severe insulin resistance in the liver and peripheral tissues, hyperinsulinemia, and diabetes mellitus. Acanthosis nigricans and hypertension have been reported in association.
Id1197746001
StatusPrimitive
Finding siteTrunk structure
Finding siteLimb structure
Associated morphologyDystrophy
Finding siteSubcutaneous fatty tissue
Finding siteStructure of endocrine system
ICD-10 complex map reference set
TargetE88.1
RuleTRUE
AdviceALWAYS E88.1 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified