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724176001: Lipodystrophy due to peptidic growth factors deficiency (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3431530019 Lipodystrophy due to peptidic growth factors deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3431531015 Lipodystrophy due to peptidic growth factors deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
3431532010 Combined insulin, insulin-like growth factor 1 and epidermal growth factor deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
3431533017 Hoepffner Dreyer Reimers syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3431534011 Werner-like syndrome due to combined growth factor deficiency en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lipodystrophy due to peptidic growth factors deficiency Is a Lipodystrophy true Inferred relationship Existential restriction modifier
Lipodystrophy due to peptidic growth factors deficiency Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 2
Lipodystrophy due to peptidic growth factors deficiency Finding site Structure of subcutaneous fatty tissue true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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