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254216006: Hereditary erythrokeratolysis (disorder)

SNOMED CT Concept\Clinical finding\...

\Functional finding\Abnormal keratinisation\Disorder of keratinisation\Inherited disorder of keratinisation\Hereditary erythrokeratolysis

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Inherited disorder of keratinisation\Hereditary erythrokeratolysis
\Integumentary system finding\Disorder of integument\Disorder of keratinisation\Inherited disorder of keratinisation\Hereditary erythrokeratolysis
\Integumentary system finding\Abnormal keratinisation\Disorder of keratinisation\Inherited disorder of keratinisation\Hereditary erythrokeratolysis

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Inherited disorder of keratinisation\Hereditary erythrokeratolysis
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Inherited disorder of keratinisation\Hereditary erythrokeratolysis
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Inherited disorder of keratinisation\Hereditary erythrokeratolysis
\Disease\Disorder of body system\Disorder of integument\Disorder of keratinisation\Inherited disorder of keratinisation\Hereditary erythrokeratolysis

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

378442016 Hereditary erythrokeratolysis en Synonym Active Case insensitive SNOMED CT core

645077011 Hereditary erythrokeratolysis (disorder) en Fully specified name Active Case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary erythrokeratolysis	Finding site	Structure of integumentary system	true	Inferred relationship	Some	2
Hereditary erythrokeratolysis	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Some	2
Hereditary erythrokeratolysis	Has definitional manifestation	Abnormal keratinisation	false	Inferred relationship	Some
Hereditary erythrokeratolysis	Associated morphology	Congenital anomaly	false	Inferred relationship	Some	1
Hereditary erythrokeratolysis	Finding site	Skin structure	false	Inferred relationship	Some	1
Hereditary erythrokeratolysis	Associated morphology	Congenital anomaly	false	Inferred relationship	Some	1
Hereditary erythrokeratolysis	Occurrence	Congenital	false	Inferred relationship	Some	2
Hereditary erythrokeratolysis	Associated morphology	Developmental abnormality	false	Inferred relationship	Some	2
Hereditary erythrokeratolysis	Finding site	Skin structure	false	Inferred relationship	Some	2
Hereditary erythrokeratolysis	Occurrence	Congenital	false	Inferred relationship	Some
Hereditary erythrokeratolysis	Finding site	Skin structure	false	Inferred relationship	Some	1
Hereditary erythrokeratolysis	Is a	Inherited disorder of keratinisation	true	Inferred relationship	Some
Hereditary erythrokeratolysis	Finding site	Structure of integumentary system	false	Inferred relationship	Some
Hereditary erythrokeratolysis	Has interpretation	Abnormal	true	Inferred relationship	Some	1
Hereditary erythrokeratolysis	Interprets	Keratinisation	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Keratolytic winter erythema	Is a	True	Hereditary erythrokeratolysis	Inferred relationship	Some
Keratolysis exfoliativa	Is a	True	Hereditary erythrokeratolysis	Inferred relationship	Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
378442016	Hereditary erythrokeratolysis	en	Synonym	Active	Case insensitive	SNOMED CT core
645077011	Hereditary erythrokeratolysis (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core