205819008: Multiple pterygium syndrome (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Skin AND/OR mucosa finding (finding)\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane (disorder)\Skin lesion\Multiple pterygium syndrome (disorder)
\Skin AND/OR mucosa finding (finding)\Skin finding\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Multiple pterygium syndrome (disorder)
\Skin AND/OR mucosa finding (finding)\Skin finding\Disorder of skin (disorder)\Skin lesion\Multiple pterygium syndrome (disorder)

\Finding of movement\Movement disorder\Multiple pterygium syndrome (disorder)
\Finding of movement\Motor dysfunction\Akinesia\Multiple pterygium syndrome (disorder)

\General finding of soft tissue\Skin finding\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Multiple pterygium syndrome (disorder)
\General finding of soft tissue\Skin finding\Disorder of skin (disorder)\Skin lesion\Multiple pterygium syndrome (disorder)
\General finding of soft tissue\Disorder of soft tissue\Lesion of soft tissue (disorder)\Skin lesion\Multiple pterygium syndrome (disorder)
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Multiple pterygium syndrome (disorder)
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin lesion\Multiple pterygium syndrome (disorder)

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument (disorder)\Multiple pterygium syndrome (disorder)
\Integumentary system finding\Disorder of integument\Disorder involving the integument of fetus OR newborn\Congenital anomaly of integument\Congenital anomaly of skin (disorder)\Multiple pterygium syndrome (disorder)
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Multiple pterygium syndrome (disorder)
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin lesion\Multiple pterygium syndrome (disorder)
\Integumentary system finding\Skin finding\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Multiple pterygium syndrome (disorder)
\Integumentary system finding\Skin finding\Disorder of skin (disorder)\Skin lesion\Multiple pterygium syndrome (disorder)

\Neurological finding\Motor nervous system finding (finding)\Motor dysfunction\Akinesia\Multiple pterygium syndrome (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of the integument (disorder)\Multiple pterygium syndrome (disorder)
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Multiple pterygium syndrome (disorder)
\Disease\Disorder of foetus and/or newborn\Disorder involving the integument of fetus OR newborn\Congenital anomaly of integument\Congenital anomaly of skin (disorder)\Multiple pterygium syndrome (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of integument\Congenital anomaly of skin (disorder)\Multiple pterygium syndrome (disorder)
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of the integument (disorder)\Multiple pterygium syndrome (disorder)
\Disease\Disorder of body system\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane (disorder)\Skin lesion\Multiple pterygium syndrome (disorder)
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument (disorder)\Multiple pterygium syndrome (disorder)
\Disease\Disorder of body system\Disorder of integument\Disorder involving the integument of fetus OR newborn\Congenital anomaly of integument\Congenital anomaly of skin (disorder)\Multiple pterygium syndrome (disorder)
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Multiple pterygium syndrome (disorder)
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin lesion\Multiple pterygium syndrome (disorder)
\Disease\Movement disorder\Multiple pterygium syndrome (disorder)
\Disease\Disorder of soft tissue\Lesion of soft tissue (disorder)\Skin lesion\Multiple pterygium syndrome (disorder)
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Multiple pterygium syndrome (disorder)
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin lesion\Multiple pterygium syndrome (disorder)
\Disease\Developmental disorder (disorder)\Developmental hereditary disorder\Multiple pterygium syndrome (disorder)
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of integument\Congenital anomaly of skin (disorder)\Multiple pterygium syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Multiple pterygium syndrome (disorder)	Is a	Congenital anomaly of limb	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple pterygium syndrome (disorder)	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple pterygium syndrome (disorder)	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple pterygium syndrome (disorder)	Finding site	Musculoskeletal structure of limb (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Multiple pterygium syndrome (disorder)	Is a	Congenital anomaly of musculoskeletal system	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple pterygium syndrome (disorder)	Finding site	Limb structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Multiple pterygium syndrome (disorder)	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Multiple pterygium syndrome (disorder)	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Multiple pterygium syndrome (disorder)	Finding site	Musculoskeletal structure of limb (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Multiple pterygium syndrome (disorder)	Is a	Disorder of musculoskeletal system (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple pterygium syndrome (disorder)	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Multiple pterygium syndrome (disorder)	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Multiple pterygium syndrome (disorder)	Finding site	Limb structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Multiple pterygium syndrome (disorder)	Is a	Arthrogryposis	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple pterygium syndrome (disorder)	Is a	Disorder of limb	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple pterygium syndrome (disorder)	Associated morphology	Contracture	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Multiple pterygium syndrome (disorder)	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Multiple pterygium syndrome (disorder)	Finding site	Joint structure of limb (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Multiple pterygium syndrome (disorder)	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Multiple pterygium syndrome (disorder)	Is a	Akinesia	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple pterygium syndrome (disorder)	Associated morphology	Congenital webbing	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Multiple pterygium syndrome (disorder)	Is a	Hereditary disorder of the integument (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple pterygium syndrome (disorder)	Is a	Congenital anomaly of skin (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple pterygium syndrome (disorder)	Finding site	Skin structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Multiple pterygium syndrome (disorder)	Is a	Skin lesion	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple pterygium syndrome (disorder)	Interprets	Movement	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Multiple pterygium syndrome (disorder)	Is a	Developmental hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Multiple pterygium syndrome (disorder)	Is a	Movement disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Lethal multiple pterygium syndrome	Is a	True	Multiple pterygium syndrome (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
X-linked lethal multiple pterygium syndrome (disorder)	Is a	True	Multiple pterygium syndrome (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Autosomal dominant multiple pterygium syndrome (disorder)	Is a	True	Multiple pterygium syndrome (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)

Reference Sets

GB English

US English

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Id	Description	Lang	Type	Status	Case?	Module
315618013	Multiple pterygium syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
591240018	Multiple pterygium syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
315618013	Multiple pterygium syndrome	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
315618013	Multiple pterygium syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
591240018	Multiple pterygium syndrome (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
591240018	Multiple pterygium syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3431831001000113	Multiples Pterygium-Syndrom	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
887961000172111	syndrome des ptérygium multiples	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
887961000172111	syndrome des ptérygium multiples	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3431831001000113	Multiples Pterygium-Syndrom	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module