715532007: Weismann Netter syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Musculoskeletal finding\Bone finding\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Bent bone dysplasia group\Weismann Netter syndrome
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Bent bone dysplasia group\Weismann Netter syndrome
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Bent bone dysplasia group\Weismann Netter syndrome
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Bent bone dysplasia group\Weismann Netter syndrome
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Bent bone dysplasia group\Weismann Netter syndrome

\Disease\Genetic disease\Weismann Netter syndrome
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Bent bone dysplasia group\Weismann Netter syndrome
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Bent bone dysplasia group\Weismann Netter syndrome
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Bent bone dysplasia group\Weismann Netter syndrome
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Bent bone dysplasia group\Weismann Netter syndrome
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Bent bone dysplasia group\Weismann Netter syndrome
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Bent bone dysplasia group\Weismann Netter syndrome
\Disease\Developmental disorder\Disorder of bone development\Congenital anomaly of skeletal bone\Bent bone dysplasia group\Weismann Netter syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Bent bone dysplasia group\Weismann Netter syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Bent bone dysplasia group\Weismann Netter syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

3302945017 Weismann Netter syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

3302947013 Weismann Netter syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

3302948015 Anterior bowing of legs with dwarfism en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Weismann Netter syndrome	Is a	Bent bone dysplasia group	true	Inferred relationship	Existential restriction modifier
Weismann Netter syndrome	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	2
Weismann Netter syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	2
Weismann Netter syndrome	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier	2
Weismann Netter syndrome	Finding site	Bone structure	true	Inferred relationship	Existential restriction modifier	1
Weismann Netter syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Weismann Netter syndrome	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	1
Weismann Netter syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Weismann Netter syndrome	Associated morphology	Dysplasia	true	Inferred relationship	Existential restriction modifier	1
Weismann Netter syndrome	Is a	Genetic disease	true	Inferred relationship	Existential restriction modifier

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
3302945017	Weismann Netter syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
3302947013	Weismann Netter syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3302948015	Anterior bowing of legs with dwarfism	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module