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766888002: Familial multiple lipomatosis (disorder)


Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3663022016 Familial multiple lipomatosis (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3663023014 Familial multiple lipomatosis en Synonym Active Case insensitive SNOMED CT core
3663027010 A rare benign genetic skin disease with characteristics of numerous, painless, encapsulated lipomas located in the subcutaneous adipose tissue of the trunk and extremities, with relative sparing of the neck and shoulders. Association with gastroduodenal lipomatosis, brain anomalies or lipomatosis, and refractory epilepsy has been reported. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial multiple lipomatosis Finding site Subcutaneous tissue structure true Inferred relationship Some 1
Familial multiple lipomatosis Is a Lipomatosis of subcutaneous tissue true Inferred relationship Some
Familial multiple lipomatosis Associated morphology Lipomatosis true Inferred relationship Some 1
Familial multiple lipomatosis Is a Familial disease true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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