724837004: Keratinopathic ichthyosis (disorder)

SNOMED CT Concept\Clinical finding\...

\Skin AND/OR mucosa finding\Skin finding\...

\Rough skin\Congenital ichthyosis of skin\Keratinopathic ichthyosis

\Disorder of skin\Keratoderma\Ichthyosis\Congenital ichthyosis of skin\Keratinopathic ichthyosis
\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Congenital ichthyosis of skin\Keratinopathic ichthyosis

\General finding of soft tissue\Skin finding\Rough skin\Congenital ichthyosis of skin\Keratinopathic ichthyosis
\General finding of soft tissue\Skin finding\Disorder of skin\Keratoderma\Ichthyosis\Congenital ichthyosis of skin\Keratinopathic ichthyosis
\General finding of soft tissue\Skin finding\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Congenital ichthyosis of skin\Keratinopathic ichthyosis
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Keratoderma\Ichthyosis\Congenital ichthyosis of skin\Keratinopathic ichthyosis
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Congenital ichthyosis of skin\Keratinopathic ichthyosis

\Functional finding\Abnormal keratinisation\...

\Rough skin\Congenital ichthyosis of skin\Keratinopathic ichthyosis

\Disorder of keratinisation\Inherited disorder of keratinisation\Congenital ichthyosis of skin\Keratinopathic ichthyosis

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Inherited disorder of keratinisation\Congenital ichthyosis of skin\Keratinopathic ichthyosis
\Integumentary system finding\Disorder of integument\Disorder of keratinisation\Inherited disorder of keratinisation\Congenital ichthyosis of skin\Keratinopathic ichthyosis
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Keratoderma\Ichthyosis\Congenital ichthyosis of skin\Keratinopathic ichthyosis
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Congenital ichthyosis of skin\Keratinopathic ichthyosis
\Integumentary system finding\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Congenital ichthyosis of skin\Keratinopathic ichthyosis
\Integumentary system finding\Skin finding\Rough skin\Congenital ichthyosis of skin\Keratinopathic ichthyosis
\Integumentary system finding\Skin finding\Disorder of skin\Keratoderma\Ichthyosis\Congenital ichthyosis of skin\Keratinopathic ichthyosis
\Integumentary system finding\Skin finding\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Congenital ichthyosis of skin\Keratinopathic ichthyosis
\Integumentary system finding\Abnormal keratinisation\Rough skin\Congenital ichthyosis of skin\Keratinopathic ichthyosis
\Integumentary system finding\Abnormal keratinisation\Disorder of keratinisation\Inherited disorder of keratinisation\Congenital ichthyosis of skin\Keratinopathic ichthyosis

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Inherited disorder of keratinisation\Congenital ichthyosis of skin\Keratinopathic ichthyosis
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Congenital ichthyosis of skin\Keratinopathic ichthyosis
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Inherited disorder of keratinisation\Congenital ichthyosis of skin\Keratinopathic ichthyosis
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Inherited disorder of keratinisation\Congenital ichthyosis of skin\Keratinopathic ichthyosis
\Disease\Disorder of body system\Disorder of integument\Disorder of keratinisation\Inherited disorder of keratinisation\Congenital ichthyosis of skin\Keratinopathic ichthyosis
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Keratoderma\Ichthyosis\Congenital ichthyosis of skin\Keratinopathic ichthyosis
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Congenital ichthyosis of skin\Keratinopathic ichthyosis
\Disease\Disorder of body system\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Congenital ichthyosis of skin\Keratinopathic ichthyosis
\Disease\Keratosis\Keratoderma\Ichthyosis\Congenital ichthyosis of skin\Keratinopathic ichthyosis
\Disease\Congenital disease\Congenital anomaly\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Congenital ichthyosis of skin\Keratinopathic ichthyosis
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Keratoderma\Ichthyosis\Congenital ichthyosis of skin\Keratinopathic ichthyosis
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Congenital ichthyosis of skin\Keratinopathic ichthyosis
\Disease\Developmental disorder\Developmental hereditary disorder\Congenital ichthyosis of skin\Keratinopathic ichthyosis
\Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Congenital ichthyosis of skin\Keratinopathic ichthyosis

Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3444917014 Keratinopathic ichthyosis (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3444918016 Keratinopathic ichthyosis en Synonym Active Case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Keratinopathic ichthyosis	Pathological process	Pathological developmental process	true	Inferred relationship	Some	1
Keratinopathic ichthyosis	Associated morphology	Hyperkeratosis	true	Inferred relationship	Some	1
Keratinopathic ichthyosis	Interprets	Keratinisation	true	Inferred relationship	Some	2
Keratinopathic ichthyosis	Has interpretation	Abnormal	true	Inferred relationship	Some	2
Keratinopathic ichthyosis	Finding site	Entire skin	true	Inferred relationship	Some	1
Keratinopathic ichthyosis	Is a	Congenital ichthyosis of skin	true	Inferred relationship	Some
Keratinopathic ichthyosis	Associated morphology	Developmental abnormality	false	Inferred relationship	Some	1
Keratinopathic ichthyosis	Occurrence	Congenital	true	Inferred relationship	Some	1
Keratinopathic ichthyosis	Finding site	Skin structure	false	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Autosomal recessive epidermolytic ichthyosis	Is a	True	Keratinopathic ichthyosis	Inferred relationship	Some
Ichthyosis hystrix of Curth-Macklin	Is a	True	Keratinopathic ichthyosis	Inferred relationship	Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3444917014	Keratinopathic ichthyosis (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3444918016	Keratinopathic ichthyosis	en	Synonym	Active	Case insensitive	SNOMED CT core