715653007: Spondyloocular syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Evaluation finding\Imaging finding\Bone densimetry abnormal\Bone density below reference range\Dysplasia with decreased bone density\Spondyloocular syndrome

\Eye / vision finding\Visual system disorder\Hereditary disorder of the visual system\Spondyloocular syndrome

\General finding of observation of patient\Procedure related finding\Bone density finding\Bone density below reference range\Dysplasia with decreased bone density\Spondyloocular syndrome

\Musculoskeletal finding\Bone finding\Bone density finding\Bone density below reference range\Dysplasia with decreased bone density\Spondyloocular syndrome
\Musculoskeletal finding\Bone finding\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Dysplasia with decreased bone density\Spondyloocular syndrome
\Musculoskeletal finding\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Spondyloocular syndrome
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Dysplasia with decreased bone density\Spondyloocular syndrome
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Dysplasia with decreased bone density\Spondyloocular syndrome
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Dysplasia with decreased bone density\Spondyloocular syndrome
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Dysplasia with decreased bone density\Spondyloocular syndrome

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the visual system\Spondyloocular syndrome
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Spondyloocular syndrome
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Spondyloocular syndrome
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Spondyloocular syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the visual system\Spondyloocular syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Spondyloocular syndrome
\Disease\Disorder of body system\Visual system disorder\Hereditary disorder of the visual system\Spondyloocular syndrome
\Disease\Disorder of body system\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Spondyloocular syndrome
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Dysplasia with decreased bone density\Spondyloocular 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\Dysplasia with decreased bone density\Spondyloocular syndrome
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Dysplasia with decreased bone density\Spondyloocular syndrome
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Dysplasia with decreased bone density\Spondyloocular syndrome
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Dysplasia with decreased bone density\Spondyloocular syndrome
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Dysplasia with decreased bone density\Spondyloocular syndrome
\Disease\Developmental disorder\Disorder of bone development\Congenital anomaly of skeletal bone\Dysplasia with decreased bone density\Spondyloocular syndrome
\Disease\Developmental disorder\Developmental hereditary disorder\Spondyloocular syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Dysplasia with decreased bone density\Spondyloocular syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Dysplasia with decreased bone density\Spondyloocular 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

3303303017 Spondyloocular syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3303304011 Spondyloocular syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3303305012 Spondylo-ocular syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Spondyloocular syndrome	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier
Spondyloocular syndrome	Is a	Dysplasia with decreased bone density	true	Inferred relationship	Existential restriction modifier
Spondyloocular syndrome	Is a	Connective tissue hereditary disorder	false	Inferred relationship	Existential restriction modifier
Spondyloocular syndrome	Is a	Hereditary disorder of musculoskeletal system	true	Inferred relationship	Existential restriction modifier
Spondyloocular syndrome	Is a	Hereditary disorder of the visual system	true	Inferred relationship	Existential restriction modifier
Spondyloocular syndrome	Finding site	Structure of visual system	true	Inferred relationship	Existential restriction modifier	1
Spondyloocular syndrome	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	3
Spondyloocular syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	3
Spondyloocular syndrome	Finding site	Bone structure	true	Inferred relationship	Existential restriction modifier	3
Spondyloocular syndrome	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	1
Spondyloocular syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	1
Spondyloocular syndrome	Pathological process	Pathological developmental process	false	Inferred relationship	Existential restriction modifier	1
Spondyloocular syndrome	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier	1
Spondyloocular syndrome	Interprets	Bone density scan	true	Inferred relationship	Existential restriction modifier	2
Spondyloocular syndrome	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier	2
Spondyloocular syndrome	Associated morphology	Dysplasia	true	Inferred relationship	Existential restriction modifier	3
Spondyloocular syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	3
Spondyloocular syndrome	Is a	Developmental hereditary disorder	true	Inferred relationship	Existential restriction modifier

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3303303017	Spondyloocular syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3303304011	Spondyloocular syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3303305012	Spondylo-ocular syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module