702342007: Dolichospondylic dysplasia (disorder)

SNOMED CT Concept\constatation clinique\...

\Musculoskeletal finding\maladie du système musculosquelettique (trouble)\...

\Hereditary disorder of musculoskeletal system\3-M syndrome

\Disorder of skeletal system\Skeletal dysplasia\3-M syndrome

\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\3-M syndrome

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\3-M syndrome
\Disease\Genetic disease\maladie héréditaire\Developmental hereditary disorder\3-M syndrome
\Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\3-M syndrome
\Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\3-M syndrome
\Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\Hereditary disorder of musculoskeletal system\3-M syndrome
\Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\Disorder of skeletal system\Skeletal dysplasia\3-M syndrome
\Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\3-M syndrome
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\3-M syndrome
\Disease\trouble du développement\Developmental hereditary disorder\3-M syndrome
\Disease\trouble du développement\Congenital malformation\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\3-M syndrome

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2995017014 3-M syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2995192019 3M syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2995591018 Dolichospondylic dysplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2995895015 Le Merrer syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2995903019 Miller-McKusick-Malvaux syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

2995927017 Dolichospondylic dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
3-M syndrome	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
3-M syndrome	morphologie associée (attribut)	dysplasie	true	Inferred relationship	Some	1
3-M syndrome	localisation d'une constatation (attribut)	Skeletal system structure	true	Inferred relationship	Some	1
3-M syndrome	est un(e) (attribut)	Developmental hereditary disorder	true	Inferred relationship	Some
3-M syndrome	est un(e) (attribut)	Connective tissue hereditary disorder	false	Inferred relationship	Some
3-M syndrome	est un(e) (attribut)	Hereditary disorder of musculoskeletal system	true	Inferred relationship	Some
3-M syndrome	est un(e) (attribut)	Skeletal dysplasia	true	Inferred relationship	Some
3-M syndrome	est un(e) (attribut)	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
3-M syndrome	survenue (attribut)	congénital	true	Inferred relationship	Some	1
3-M syndrome	localisation d'une constatation (attribut)	structure osseuse	false	Inferred relationship	Some	1
3-M syndrome	morphologie associée (attribut)	Congenital dysplasia	false	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets