279081001: Dysostosis multiplex group (disorder)

SNOMED CT Concept\Clinical finding\...

\Musculoskeletal finding\Bone finding\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Dysostosis multiplex group
\Musculoskeletal finding\Bone finding\Disorder of bone\Metabolic bone disease\Dysostosis multiplex group
\Musculoskeletal finding\Musculoskeletal disorder\Hereditary disorder of musculoskeletal system\Dysostosis multiplex group
\Musculoskeletal finding\Musculoskeletal disorder\Disorder of skeletal system\Congenital skeletal dysplasia\Dysostosis multiplex group
\Musculoskeletal finding\Musculoskeletal disorder\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Dysostosis multiplex group
\Musculoskeletal finding\Musculoskeletal disorder\Disorder of skeletal system\Disorder of bone\Metabolic bone disease\Dysostosis multiplex group
\Musculoskeletal finding\Musculoskeletal disorder\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Dysostosis multiplex group
\Musculoskeletal finding\Musculoskeletal disorder\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Dysostosis multiplex group

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Dysostosis multiplex group
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Dysostosis multiplex group
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Dysostosis multiplex group
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Dysostosis multiplex group
\Disease\Disorder of body system\Musculoskeletal disorder\Hereditary disorder of musculoskeletal system\Dysostosis multiplex group
\Disease\Disorder of body system\Musculoskeletal disorder\Disorder of skeletal system\Congenital skeletal dysplasia\Dysostosis multiplex group
\Disease\Disorder of body system\Musculoskeletal disorder\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Dysostosis multiplex group
\Disease\Disorder of body system\Musculoskeletal disorder\Disorder of skeletal system\Disorder of bone\Metabolic bone disease\Dysostosis multiplex group
\Disease\Disorder of body system\Musculoskeletal disorder\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Dysostosis multiplex group
\Disease\Disorder of body system\Musculoskeletal disorder\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Dysostosis multiplex group
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Dysostosis multiplex group
\Disease\Metabolic disease\Enzymopathy\Disorder of lysosomal enzyme\Dysostosis multiplex group
\Disease\Metabolic disease\Metabolic bone disease\Dysostosis multiplex group
\Disease\Congenital disease\Congenital anomaly\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Dysostosis multiplex group
\Disease\Congenital disease\Congenital anomaly\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Dysostosis multiplex group
\Disease\Congenital disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Dysostosis multiplex group
\Disease\Developmental disorder\Disorder of bone development\Congenital anomaly of skeletal bone\Dysostosis multiplex group
\Disease\Developmental disorder\Developmental hereditary disorder\Dysostosis multiplex group
\Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Dysostosis multiplex group
\Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Dysostosis multiplex group

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

416203012 Dysostosis multiplex group en Synonym Active Case insensitive SNOMED CT core

672320018 Dysostosis multiplex group (disorder) en Fully specified name Active Case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Dysostosis multiplex group	Occurrence	Congenital	true	Inferred relationship	Some	1
Dysostosis multiplex group	Pathological process	Pathological developmental process	true	Inferred relationship	Some	1
Dysostosis multiplex group	Is a	Congenital anomaly of skeletal bone	true	Inferred relationship	Some
Dysostosis multiplex group	Is a	Developmental hereditary disorder	true	Inferred relationship	Some
Dysostosis multiplex group	Associated morphology	Congenital dysplasia	false	Inferred relationship	Some	1
Dysostosis multiplex group	Is a	Metabolic bone disease	true	Inferred relationship	Some
Dysostosis multiplex group	Is a	Inherited disorder of connective tissue	false	Inferred relationship	Some
Dysostosis multiplex group	Finding site	Bone structure	false	Inferred relationship	Some	1
Dysostosis multiplex group	Associated morphology	Congenital dysplasia	false	Inferred relationship	Some	1
Dysostosis multiplex group	Occurrence	Congenital	false	Inferred relationship	Some	2
Dysostosis multiplex group	Finding site	Bone structure	false	Inferred relationship	Some	2
Dysostosis multiplex group	Associated morphology	Congenital dysplasia	false	Inferred relationship	Some	2
Dysostosis multiplex group	Associated morphology	Dysplasia	true	Inferred relationship	Some	1
Dysostosis multiplex group	Finding site	Skeletal system structure	false	Inferred relationship	Some	1
Dysostosis multiplex group	Occurrence	Congenital	false	Inferred relationship	Some
Dysostosis multiplex group	Finding site	Bone structure	true	Inferred relationship	Some	1
Dysostosis multiplex group	Is a	Disorder of lysosomal enzyme	true	Inferred relationship	Some
Dysostosis multiplex group	Is a	Congenital skeletal dysplasia	true	Inferred relationship	Some
Dysostosis multiplex group	Is a	Hereditary disorder of musculoskeletal system	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Mucopolysaccharidosis-like plus disease	Is a	True	Dysostosis multiplex group	Inferred relationship	Some
Combined deficiency of sialidase AND beta galactosidase	Is a	True	Dysostosis multiplex group	Inferred relationship	Some
Aspartylglucosaminuria	Is a	False	Dysostosis multiplex group	Inferred relationship	Some
Fucosidosis	Is a	False	Dysostosis multiplex group	Inferred relationship	Some
Mannosidosis	Is a	True	Dysostosis multiplex group	Inferred relationship	Some
I-cell disease	Is a	True	Dysostosis multiplex group	Inferred relationship	Some
Dysostosis multiplex	Is a	True	Dysostosis multiplex group	Inferred relationship	Some
GM1 gangliosidosis	Is a	True	Dysostosis multiplex group	Inferred relationship	Some
Ganglioside sialidase deficiency	Is a	False	Dysostosis multiplex group	Inferred relationship	Some
Sialic storage disease	Is a	True	Dysostosis multiplex group	Inferred relationship	Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
416203012	Dysostosis multiplex group	en	Synonym	Active	Case insensitive	SNOMED CT core
672320018	Dysostosis multiplex group (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core