58112007: Mannosidosis, type II (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\Mannosidosis\Mannosidosis, type II
\Musculoskeletal finding\Bone finding\Disorder of bone\Metabolic bone disease\Dysostosis multiplex group\Mannosidosis\Mannosidosis, type II
\Musculoskeletal finding\Musculoskeletal disorder\Hereditary disorder of musculoskeletal system\Dysostosis multiplex group\Mannosidosis\Mannosidosis, type II
\Musculoskeletal finding\Musculoskeletal disorder\Disorder of skeletal system\Congenital skeletal dysplasia\Dysostosis multiplex group\Mannosidosis\Mannosidosis, type II
\Musculoskeletal finding\Musculoskeletal disorder\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Dysostosis multiplex group\Mannosidosis\Mannosidosis, type II
\Musculoskeletal finding\Musculoskeletal disorder\Disorder of skeletal system\Disorder of bone\Metabolic bone disease\Dysostosis multiplex group\Mannosidosis\Mannosidosis, type II
\Musculoskeletal finding\Musculoskeletal disorder\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Dysostosis multiplex group\Mannosidosis\Mannosidosis, type II
\Musculoskeletal finding\Musculoskeletal disorder\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Dysostosis multiplex group\Mannosidosis\Mannosidosis, type II

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

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

Descriptions:

Id Description Lang Type Status Case? Module

1231806011 Juvenile mannosidosis en Synonym Active Case insensitive SNOMED CT core

796809018 Mannosidosis, type II (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core

96576013 Mannosidosis, type II en Synonym Active Initial character case insensitive SNOMED CT core

96577016 Mannosidosis, juvenile-adult onset en Synonym Active Case insensitive SNOMED CT core

96578014 Mannosidosis, mild form en Synonym Active Case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Mannosidosis, type II	Occurrence	Congenital	true	Inferred relationship	Some	1
Mannosidosis, type II	Pathological process	Pathological developmental process	true	Inferred relationship	Some	1
Mannosidosis, type II	Associated morphology	Congenital dysplasia	false	Inferred relationship	Some	1
Mannosidosis, type II	Is a	Mannosidosis	true	Inferred relationship	Some
Mannosidosis, type II	Associated morphology	Congenital dysplasia	false	Inferred relationship	Some	1
Mannosidosis, type II	Finding site	Bone structure	false	Inferred relationship	Some	1
Mannosidosis, type II	Occurrence	Congenital	false	Inferred relationship	Some	2
Mannosidosis, type II	Finding site	Bone structure	false	Inferred relationship	Some	2
Mannosidosis, type II	Associated morphology	Congenital dysplasia	false	Inferred relationship	Some	2
Mannosidosis, type II	Occurrence	Congenital	false	Inferred relationship	Some
Mannosidosis, type II	Severity	Mild	false	Inferred relationship	Some
Mannosidosis, type II	Finding site	Skeletal system structure	false	Inferred relationship	Some	1
Mannosidosis, type II	Associated morphology	Dysplasia	true	Inferred relationship	Some	1
Mannosidosis, type II	Finding site	Bone structure	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
1231806011	Juvenile mannosidosis	en	Synonym	Active	Case insensitive	SNOMED CT core
796809018	Mannosidosis, type II (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
96576013	Mannosidosis, type II	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
96577016	Mannosidosis, juvenile-adult onset	en	Synonym	Active	Case insensitive	SNOMED CT core
96578014	Mannosidosis, mild form	en	Synonym	Active	Case insensitive	SNOMED CT core