58263000: Maroteaux-Lamy syndrome, severe form (disorder)

SNOMED CT Concept\Clinical finding\...

\Finding of general physiological development\Disorder of stature\Short stature disorder\Maroteaux-Lamy syndrome\Maroteaux-Lamy syndrome, severe form

\General finding of observation of patient\Body measurement finding\Height / growth finding\General finding of height\Disorder of stature\Short stature disorder\Maroteaux-Lamy syndrome\Maroteaux-Lamy syndrome, severe form

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited metabolic disorder of nervous system\Deficiency of cerebroside-sulfatase\Deficiency of N-acetylgalactosamine-4-sulfatase\Maroteaux-Lamy syndrome\Maroteaux-Lamy syndrome, severe form
\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Deficiency of cerebroside-sulfatase\Deficiency of N-acetylgalactosamine-4-sulfatase\Maroteaux-Lamy syndrome\Maroteaux-Lamy syndrome, severe form
\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Mucopolysaccharidosis\Maroteaux-Lamy syndrome\Maroteaux-Lamy syndrome, severe form
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Deficiency of cerebroside-sulfatase\Deficiency of N-acetylgalactosamine-4-sulfatase\Maroteaux-Lamy syndrome\Maroteaux-Lamy syndrome, severe form
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Maroteaux-Lamy syndrome\Maroteaux-Lamy syndrome, severe form
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Maroteaux-Lamy syndrome\Maroteaux-Lamy syndrome, severe form
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Deficiency of cerebroside-sulfatase\Deficiency of N-acetylgalactosamine-4-sulfatase\Maroteaux-Lamy syndrome\Maroteaux-Lamy syndrome, severe form
\Disease\Disorder of body system\Disorder of nervous system\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Deficiency of cerebroside-sulfatase\Deficiency of N-acetylgalactosamine-4-sulfatase\Maroteaux-Lamy syndrome\Maroteaux-Lamy syndrome, severe form
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited metabolic disorder of nervous system\Deficiency of cerebroside-sulfatase\Deficiency of N-acetylgalactosamine-4-sulfatase\Maroteaux-Lamy syndrome\Maroteaux-Lamy syndrome, severe form
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Deficiency of cerebroside-sulfatase\Deficiency of N-acetylgalactosamine-4-sulfatase\Maroteaux-Lamy syndrome\Maroteaux-Lamy syndrome, severe form
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Mucopolysaccharidosis\Maroteaux-Lamy syndrome\Maroteaux-Lamy syndrome, severe form
\Disease\Metabolic disease\Enzymopathy\Disorder of lysosomal enzyme\Deficiency of cerebroside-sulfatase\Deficiency of N-acetylgalactosamine-4-sulfatase\Maroteaux-Lamy syndrome\Maroteaux-Lamy syndrome, severe form
\Disease\Metabolic disease\Enzymopathy\Disorder of lysosomal enzyme\Mucopolysaccharidosis\Maroteaux-Lamy syndrome\Maroteaux-Lamy syndrome, severe form
\Disease\Congenital disease\Inborn error of metabolism\Inherited metabolic disorder of nervous system\Deficiency of cerebroside-sulfatase\Deficiency of N-acetylgalactosamine-4-sulfatase\Maroteaux-Lamy syndrome\Maroteaux-Lamy syndrome, severe form
\Disease\Congenital disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Deficiency of cerebroside-sulfatase\Deficiency of N-acetylgalactosamine-4-sulfatase\Maroteaux-Lamy syndrome\Maroteaux-Lamy syndrome, severe form
\Disease\Congenital disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Mucopolysaccharidosis\Maroteaux-Lamy syndrome\Maroteaux-Lamy syndrome, severe form
\Disease\Developmental disorder\Developmental hereditary disorder\Maroteaux-Lamy syndrome\Maroteaux-Lamy syndrome, severe form
\Disease\Developmental disorder\Disorder of stature\Short stature disorder\Maroteaux-Lamy syndrome\Maroteaux-Lamy syndrome, severe form

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

Descriptions:

Id Description Lang Type Status Case? Module

96831018 Maroteaux-Lamy syndrome, severe form en Synonym Active Entire term case sensitive SNOMED CT core module

796976010 Maroteaux-Lamy syndrome, severe form (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Maroteaux-Lamy syndrome, severe form	Is a	Maroteaux-Lamy syndrome	true	Inferred relationship	Existential restriction modifier
Maroteaux-Lamy syndrome, severe form	Finding site	Structure of nervous system	false	Inferred relationship	Existential restriction modifier	2
Maroteaux-Lamy syndrome, severe form	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Maroteaux-Lamy syndrome, severe form	Severity	Severe	false	Inferred relationship	Existential restriction modifier
Maroteaux-Lamy syndrome, severe form	Pathological process	Pathological developmental process	false	Inferred relationship	Existential restriction modifier	3
Maroteaux-Lamy syndrome, severe form	Finding site	Structure of nervous system	true	Inferred relationship	Existential restriction modifier	1
Maroteaux-Lamy syndrome, severe form	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Maroteaux-Lamy syndrome, severe form	Interprets	Height / growth measure	true	Inferred relationship	Existential restriction modifier	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
96831018	Maroteaux-Lamy syndrome, severe form	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
796976010	Maroteaux-Lamy syndrome, severe form (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module