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725164008: Omodysplasia (disorder)

SNOMED CT Concept\Clinical finding\...

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

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

Descriptions:

Id Description Lang Type Status Case? Module

3439905012 Omodysplasia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3439906013 Omodysplasia en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Omodysplasia	Is a	Autosomal hereditary disorder	true	Inferred relationship	Existential restriction modifier
Omodysplasia	Is a	Congenital skeletal dysplasia	true	Inferred relationship	Existential restriction modifier
Omodysplasia	Is a	Connective tissue hereditary disorder	false	Inferred relationship	Existential restriction modifier
Omodysplasia	Is a	Hereditary disorder of musculoskeletal system	true	Inferred relationship	Existential restriction modifier
Omodysplasia	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	1
Omodysplasia	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Omodysplasia	Finding site	Bone structure	true	Inferred relationship	Existential restriction modifier	1
Omodysplasia	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Omodysplasia	Associated morphology	Dysplasia	true	Inferred relationship	Existential restriction modifier	1
Omodysplasia	Is a	Congenital anomaly of skeletal bone	true	Inferred relationship	Existential restriction modifier
Omodysplasia	Is a	Developmental hereditary disorder	true	Inferred relationship	Existential restriction modifier

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Autosomal dominant omodysplasia	Is a	True	Omodysplasia	Inferred relationship	Existential restriction modifier
Autosomal recessive omodysplasia	Is a	True	Omodysplasia	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3439905012	Omodysplasia (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3439906013	Omodysplasia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module