719304005: Spondylometaphyseal dysplasia Schmidt type (disorder)

SNOMED CT Concept\Clinical finding\...

\Musculoskeletal finding\Bone finding\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Spondylometaphyseal dysplasia Schmidt type
\Musculoskeletal finding\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Spondylometaphyseal dysplasia\Spondylometaphyseal dysplasia Schmidt type
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Spondylometaphyseal dysplasia\Spondylometaphyseal dysplasia Schmidt type
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Spondylometaphyseal dysplasia Schmidt type
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Spondylometaphyseal dysplasia\Spondylometaphyseal dysplasia Schmidt type
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Spondylometaphyseal dysplasia Schmidt type

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Spondylometaphyseal dysplasia\Spondylometaphyseal dysplasia Schmidt type
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Spondylometaphyseal dysplasia\Spondylometaphyseal dysplasia Schmidt type
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Spondylometaphyseal dysplasia Schmidt type
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Spondylometaphyseal dysplasia\Spondylometaphyseal dysplasia Schmidt type
\Disease\Disorder of body system\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Spondylometaphyseal dysplasia\Spondylometaphyseal dysplasia Schmidt type
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Spondylometaphyseal dysplasia\Spondylometaphyseal dysplasia Schmidt type
\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\Spondylometaphyseal dysplasia Schmidt type
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Spondylometaphyseal dysplasia\Spondylometaphyseal dysplasia Schmidt type
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Spondylometaphyseal dysplasia Schmidt type
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Spondylometaphyseal dysplasia\Spondylometaphyseal dysplasia Schmidt type
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Spondylometaphyseal dysplasia Schmidt type
\Disease\Developmental disorder\Disorder of bone development\Congenital anomaly of skeletal bone\Spondylometaphyseal dysplasia Schmidt type
\Disease\Developmental disorder\Developmental hereditary disorder\Spondylometaphyseal dysplasia\Spondylometaphyseal dysplasia Schmidt type
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Spondylometaphyseal dysplasia\Spondylometaphyseal dysplasia Schmidt type
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Spondylometaphyseal dysplasia Schmidt type

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

3315922014 Spondylometaphyseal dysplasia Schmidt type (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

3315923016 Spondylometaphyseal dysplasia Schmidt type en Synonym Active Only initial character case insensitive SNOMED CT core module

3315924010 Spondylometaphyseal dysplasia with severe genu valgum en Synonym Active Entire term case insensitive SNOMED CT core module

3315925011 Spondylometaphyseal dysplasia Algerian type en Synonym Active Only initial character case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Spondylometaphyseal dysplasia Schmidt type	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier
Spondylometaphyseal dysplasia Schmidt type	Is a	Metaphyseal chondrodysplasia	false	Inferred relationship	Existential restriction modifier
Spondylometaphyseal dysplasia Schmidt type	Is a	Short stature disorder	false	Inferred relationship	Existential restriction modifier
Spondylometaphyseal dysplasia Schmidt type	Is a	Connective tissue hereditary disorder	false	Inferred relationship	Existential restriction modifier
Spondylometaphyseal dysplasia Schmidt type	Is a	Hereditary disorder of musculoskeletal system	false	Inferred relationship	Existential restriction modifier
Spondylometaphyseal dysplasia Schmidt type	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	2
Spondylometaphyseal dysplasia Schmidt type	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	2
Spondylometaphyseal dysplasia Schmidt type	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier	2
Spondylometaphyseal dysplasia Schmidt type	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	1
Spondylometaphyseal dysplasia Schmidt type	Finding site	Bone structure	true	Inferred relationship	Existential restriction modifier	1
Spondylometaphyseal dysplasia Schmidt type	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Spondylometaphyseal dysplasia Schmidt type	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Spondylometaphyseal dysplasia Schmidt type	Associated morphology	Dysplasia	true	Inferred relationship	Existential restriction modifier	1
Spondylometaphyseal dysplasia Schmidt type	Is a	Spondylometaphyseal dysplasia	true	Inferred relationship	Existential restriction modifier
Spondylometaphyseal dysplasia Schmidt type	Is a	Congenital anomaly of skeletal bone	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
3315922014	Spondylometaphyseal dysplasia Schmidt type (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
3315923016	Spondylometaphyseal dysplasia Schmidt type	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3315924010	Spondylometaphyseal dysplasia with severe genu valgum	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3315925011	Spondylometaphyseal dysplasia Algerian type	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module