111388003: Cutis laxa, autosomal dominant (disorder)

SNOMED CT Concept\Clinical finding\...

\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Collagen and elastic tissue disorders affecting skin\Cutis laxa\Inherited cutis laxa\Cutis laxa, autosomal dominant

\General finding of soft tissue\Skin finding\Disorder of skin\Collagen and elastic tissue disorders affecting skin\Cutis laxa\Inherited cutis laxa\Cutis laxa, autosomal dominant
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Collagen and elastic tissue disorders affecting skin\Cutis laxa\Inherited cutis laxa\Cutis laxa, autosomal dominant

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Inherited cutis laxa\Cutis laxa, autosomal dominant
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Collagen and elastic tissue disorders affecting skin\Cutis laxa\Inherited cutis laxa\Cutis laxa, autosomal dominant
\Integumentary system finding\Skin finding\Disorder of skin\Collagen and elastic tissue disorders affecting skin\Cutis laxa\Inherited cutis laxa\Cutis laxa, autosomal dominant

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Inherited cutis laxa\Cutis laxa, autosomal dominant
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Inherited cutis laxa\Cutis laxa, autosomal dominant
\Disease\Genetic disease\Hereditary disease\Inherited disorder of connective tissue\Inherited cutis laxa\Cutis laxa, autosomal dominant
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Cutis laxa, autosomal dominant
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Inherited cutis laxa\Cutis laxa, autosomal dominant
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Inherited cutis laxa\Cutis laxa, autosomal dominant
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Collagen and elastic tissue disorders affecting skin\Cutis laxa\Inherited cutis laxa\Cutis laxa, autosomal dominant
\Disease\Disorder of connective tissue\Inherited disorder of connective tissue\Inherited cutis laxa\Cutis laxa, autosomal dominant
\Disease\Disorder of connective tissue\Congenital connective tissue disorder\Inherited cutis laxa\Cutis laxa, autosomal dominant
\Disease\Disorder of connective tissue\Metabolic disease of collagen\Cutis laxa\Inherited cutis laxa\Cutis laxa, autosomal dominant
\Disease\Metabolic disease\Metabolic disease of collagen\Cutis laxa\Inherited cutis laxa\Cutis laxa, autosomal dominant
\Disease\Congenital disease\Congenital connective tissue disorder\Inherited cutis laxa\Cutis laxa, autosomal dominant
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Collagen and elastic tissue disorders affecting skin\Cutis laxa\Inherited cutis laxa\Cutis laxa, autosomal dominant
\Disease\Developmental disorder\Developmental hereditary disorder\Inherited cutis laxa\Cutis laxa, autosomal dominant

Status: current, Defined. Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

178628015 Cutis laxa, autosomal dominant en Synonym Active Case insensitive SNOMED CT core

630983013 Cutis laxa, autosomal dominant (disorder) en Fully specified name Active Case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Cutis laxa, autosomal dominant	Associated morphology	Morphologically abnormal structure	false	Inferred relationship	Some	1
Cutis laxa, autosomal dominant	Pathological process	Pathological developmental process	true	Inferred relationship	Some	1
Cutis laxa, autosomal dominant	Occurrence	Congenital	true	Inferred relationship	Some	1
Cutis laxa, autosomal dominant	Finding site	Connective tissue structure	true	Inferred relationship	Some	1
Cutis laxa, autosomal dominant	Associated morphology	Congenital anomaly	false	Inferred relationship	Some	1
Cutis laxa, autosomal dominant	Is a	Hereditary disorder of the integument	false	Inferred relationship	Some
Cutis laxa, autosomal dominant	Is a	Inherited disorder of connective tissue	false	Inferred relationship	Some
Cutis laxa, autosomal dominant	Associated morphology	Congenital anomaly	false	Inferred relationship	Some	1
Cutis laxa, autosomal dominant	Finding site	Skin structure	false	Inferred relationship	Some	1
Cutis laxa, autosomal dominant	Occurrence	Congenital	false	Inferred relationship	Some	2
Cutis laxa, autosomal dominant	Associated morphology	Developmental abnormality	false	Inferred relationship	Some	2
Cutis laxa, autosomal dominant	Finding site	Skin structure	true	Inferred relationship	Some	2
Cutis laxa, autosomal dominant	Finding site	Structure of musculoskeletal system	false	Inferred relationship	Some
Cutis laxa, autosomal dominant	Finding site	Connective tissue structure	false	Inferred relationship	Some
Cutis laxa, autosomal dominant	Occurrence	Congenital	false	Inferred relationship	Some
Cutis laxa, autosomal dominant	Finding site	Skin structure	false	Inferred relationship	Some	1
Cutis laxa, autosomal dominant	Finding site	Connective tissue	false	Inferred relationship	Some
Cutis laxa, autosomal dominant	Is a	Inherited cutis laxa	true	Inferred relationship	Some
Cutis laxa, autosomal dominant	Is a	Autosomal dominant 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

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
178628015	Cutis laxa, autosomal dominant	en	Synonym	Active	Case insensitive	SNOMED CT core
630983013	Cutis laxa, autosomal dominant (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core