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419395007: Schnyder crystalline cornea dystrophy (disorder)


Status: current, Primitive. Date: 31-Jan 2006. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2574207014 Schnyder crystalline cornea dystrophy (disorder) en Fully specified name Active Case sensitive SNOMED CT core
2577547014 Schnyder crystalline cornea dystrophy en Synonym Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Schnyder crystalline cornea dystrophy Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Schnyder crystalline cornea dystrophy Is a Stromal corneal dystrophy true Inferred relationship Some
Schnyder crystalline cornea dystrophy Is a Inherited disorder of connective tissue true Inferred relationship Some
Schnyder crystalline cornea dystrophy Is a Hereditary corneal dystrophy true Inferred relationship Some
Schnyder crystalline cornea dystrophy Finding site Structure of substantia propria of cornea true Inferred relationship Some 1
Schnyder crystalline cornea dystrophy Associated morphology Dystrophy false Inferred relationship Some 1
Schnyder crystalline cornea dystrophy Finding site Structure of substantia propria of cornea false Inferred relationship Some 1
Schnyder crystalline cornea dystrophy Associated morphology Dystrophy true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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