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1197746001: AKT serine/threonine kinase 2-related familial partial lipodystrophy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 28-Feb 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4697877010 AKT serine/threonine kinase 2-related familial partial lipodystrophy en Synonym Active Entire term case sensitive SNOMED CT core module
4697878017 AKT2-related familial partial lipodystrophy en Synonym Active Entire term case sensitive SNOMED CT core module
4697879013 AKT serine/threonine kinase 2-related familial partial lipodystrophy (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
AKT serine/threonine kinase 2-related familial partial lipodystrophy Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
AKT serine/threonine kinase 2-related familial partial lipodystrophy Is a Connective tissue hereditary disorder true Inferred relationship Existential restriction modifier
AKT serine/threonine kinase 2-related familial partial lipodystrophy Is a Hereditary disorder of the integument true Inferred relationship Existential restriction modifier
AKT serine/threonine kinase 2-related familial partial lipodystrophy Is a Familial partial lipodystrophy true Inferred relationship Existential restriction modifier
AKT serine/threonine kinase 2-related familial partial lipodystrophy Finding site Trunk structure true Inferred relationship Existential restriction modifier 2
AKT serine/threonine kinase 2-related familial partial lipodystrophy Finding site Limb structure true Inferred relationship Existential restriction modifier 3
AKT serine/threonine kinase 2-related familial partial lipodystrophy Finding site Structure of subcutaneous fatty tissue true Inferred relationship Existential restriction modifier 1
AKT serine/threonine kinase 2-related familial partial lipodystrophy Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
AKT serine/threonine kinase 2-related familial partial lipodystrophy Is a Hereditary disorder of endocrine system true Inferred relationship Existential restriction modifier
AKT serine/threonine kinase 2-related familial partial lipodystrophy Finding site Structure of endocrine system true Inferred relationship Existential restriction modifier 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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