254094003: Dysplasias with significant membranous bone involvement (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Musculoskeletal finding\Bone finding\Disorder of bone (disorder)\Disorder of bone development (disorder)\Congenital anomaly of skeletal bone\Dysplasias with significant membranous bone involvement
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Skeletal dysplasia\Dysplasias with significant membranous bone involvement
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone (disorder)\Disorder of bone development (disorder)\Congenital anomaly of skeletal bone\Dysplasias with significant membranous bone involvement
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\Dysplasias with significant membranous bone involvement
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Dysplasias with significant membranous bone involvement

\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Skeletal dysplasia\Dysplasias with significant membranous bone involvement
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone (disorder)\Disorder of bone development (disorder)\Congenital anomaly of skeletal bone\Dysplasias with significant membranous bone involvement
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\Dysplasias with significant membranous bone involvement
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Dysplasias with significant membranous bone involvement
\Disease\Congenital disease (disorder)\Congenital malformation\Congenital malformation syndrome (disorder)\Multiple system malformation syndrome\Osteochondrodysplasia syndrome\Dysplasias with significant membranous bone involvement
\Disease\Congenital disease (disorder)\Congenital malformation\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\Dysplasias with significant membranous bone involvement
\Disease\Congenital disease (disorder)\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Dysplasias with significant membranous bone involvement
\Disease\Developmental disorder\Disorder of bone development (disorder)\Congenital anomaly of skeletal bone\Dysplasias with significant membranous bone involvement
\Disease\Developmental disorder\Congenital malformation\Congenital malformation syndrome (disorder)\Multiple system malformation syndrome\Osteochondrodysplasia syndrome\Dysplasias with significant membranous bone involvement
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\Dysplasias with significant membranous bone involvement
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Dysplasias with significant membranous bone involvement

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

378251010 Dysplasias with significant membranous bone involvement en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

644938016 Dysplasias with significant membranous bone involvement (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1986721000052117 dysplasier med signifikant membranöst skelettengagemang sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Dysplasias with significant membranous bone involvement	Is a	Osteochondrodysplasia syndrome	true	Inferred relationship	Some
Dysplasias with significant membranous bone involvement	Is a	Skeletal dysplasia	true	Inferred relationship	Some
Dysplasias with significant membranous bone involvement	Associated morphology	Dysplasia	true	Inferred relationship	Some	1
Dysplasias with significant membranous bone involvement	Occurrence	Congenital	false	Inferred relationship	Some
Dysplasias with significant membranous bone involvement	Finding site	Bone structure	true	Inferred relationship	Some	1
Dysplasias with significant membranous bone involvement	Finding site	Skeletal system structure	false	Inferred relationship	Some	1
Dysplasias with significant membranous bone involvement	Associated morphology	kongenital dysplasi	false	Inferred relationship	Some	1
Dysplasias with significant membranous bone involvement	Associated morphology	medfödd missbildning	false	Inferred relationship	Some
Dysplasias with significant membranous bone involvement	Associated morphology	kongenital dysplasi	false	Inferred relationship	Some	1
Dysplasias with significant membranous bone involvement	Finding site	Bone structure	false	Inferred relationship	Some	1
Dysplasias with significant membranous bone involvement	Occurrence	Congenital	false	Inferred relationship	Some	2
Dysplasias with significant membranous bone involvement	Finding site	Bone structure	false	Inferred relationship	Some	2
Dysplasias with significant membranous bone involvement	Associated morphology	kongenital dysplasi	false	Inferred relationship	Some	2
Dysplasias with significant membranous bone involvement	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Dysplasias with significant membranous bone involvement	Occurrence	Congenital	true	Inferred relationship	Some	1
Dysplasias with significant membranous bone involvement	Is a	Congenital anomaly of skeletal bone	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Melnick-Needles syndrome	Is a	False	Dysplasias with significant membranous bone involvement	Inferred relationship	Some
Cleidocranial dysostosis	Is a	False	Dysplasias with significant membranous bone involvement	Inferred relationship	Some
Yunis-Varon dysplasia (disorder)	Is a	True	Dysplasias with significant membranous bone involvement	Inferred relationship	Some
Precocious osteodysplasty (disorder)	Is a	True	Dysplasias with significant membranous bone involvement	Inferred relationship	Some

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
378251010	Dysplasias with significant membranous bone involvement	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
644938016	Dysplasias with significant membranous bone involvement (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1986721000052117	dysplasier med signifikant membranöst skelettengagemang	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)