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709490002: Desmosterolosis (disorder)


Status: current, Primitive. Date: 31-Jul 2015. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3039582016 Desmosterolosis (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3040185019 Desmosterolosis en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Desmosterolosis Interprets Bone density scan true Inferred relationship Some 2
Desmosterolosis Associated morphology Dysplasia true Inferred relationship Some 1
Desmosterolosis Pathological process Pathological developmental process true Inferred relationship Some 1
Desmosterolosis Finding site Bone structure true Inferred relationship Some 1
Desmosterolosis Is a Neonatal osteosclerotic dysplasia true Inferred relationship Some
Desmosterolosis Is a Metabolic bone disease true Inferred relationship Some
Desmosterolosis Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Desmosterolosis Has interpretation Above reference range true Inferred relationship Some 2
Desmosterolosis Occurrence Congenital true Inferred relationship Some 1
Desmosterolosis Is a Developmental hereditary disorder true Inferred relationship Some
Desmosterolosis Is a Disorder of cholesterol synthesis true Inferred relationship Some
Desmosterolosis Is a Autosomal recessive hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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