238019007: Total hexosaminidase deficiency - juvenile (disorder)

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

\Genetic disease\Hereditary disease\...

\Hereditary disorder by system\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Gangliosidosis\GM2 gangliosidosis (disorder)\...

\Sandhoff disease\Total hexosaminidase deficiency - juvenile

\Juvenile GM2 gangliosidosis (disorder)\Total hexosaminidase deficiency - juvenile

\Inborn error of metabolism\Inherited metabolic disorder of nervous system\Gangliosidosis\GM2 gangliosidosis (disorder)\Sandhoff disease\Total hexosaminidase deficiency - juvenile
\Inborn error of metabolism\Inherited metabolic disorder of nervous system\Gangliosidosis\GM2 gangliosidosis (disorder)\Juvenile GM2 gangliosidosis (disorder)\Total hexosaminidase deficiency - juvenile
\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Gangliosidosis\GM2 gangliosidosis (disorder)\Sandhoff disease\Total hexosaminidase deficiency - juvenile
\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Gangliosidosis\GM2 gangliosidosis (disorder)\Juvenile GM2 gangliosidosis (disorder)\Total hexosaminidase deficiency - juvenile

\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Gangliosidosis\GM2 gangliosidosis (disorder)\Sandhoff disease\Total hexosaminidase deficiency - juvenile
\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Gangliosidosis\GM2 gangliosidosis (disorder)\Juvenile GM2 gangliosidosis (disorder)\Total hexosaminidase deficiency - juvenile
\Disorder of body system\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Gangliosidosis\GM2 gangliosidosis (disorder)\Sandhoff disease\Total hexosaminidase deficiency - juvenile
\Disorder of body system\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Gangliosidosis\GM2 gangliosidosis (disorder)\Juvenile GM2 gangliosidosis (disorder)\Total hexosaminidase deficiency - juvenile

\Metabolic disease\Inborn error of metabolism\Inherited metabolic disorder of nervous system\Gangliosidosis\GM2 gangliosidosis (disorder)\Sandhoff disease\Total hexosaminidase deficiency - juvenile
\Metabolic disease\Inborn error of metabolism\Inherited metabolic disorder of nervous system\Gangliosidosis\GM2 gangliosidosis (disorder)\Juvenile GM2 gangliosidosis (disorder)\Total hexosaminidase deficiency - juvenile
\Metabolic disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Gangliosidosis\GM2 gangliosidosis (disorder)\Sandhoff disease\Total hexosaminidase deficiency - juvenile
\Metabolic disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Gangliosidosis\GM2 gangliosidosis (disorder)\Juvenile GM2 gangliosidosis (disorder)\Total hexosaminidase deficiency - juvenile
\Metabolic disease\Enzymopathy\Disorder of lysosomal enzyme\Gangliosidosis\GM2 gangliosidosis (disorder)\Sandhoff disease\Total hexosaminidase deficiency - juvenile
\Metabolic disease\Enzymopathy\Disorder of lysosomal enzyme\Gangliosidosis\GM2 gangliosidosis (disorder)\Juvenile GM2 gangliosidosis (disorder)\Total hexosaminidase deficiency - juvenile
\Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of lipid storage and metabolism\Gangliosidosis\GM2 gangliosidosis (disorder)\Sandhoff disease\Total hexosaminidase deficiency - juvenile
\Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of lipid storage and metabolism\Gangliosidosis\GM2 gangliosidosis (disorder)\Juvenile GM2 gangliosidosis (disorder)\Total hexosaminidase deficiency - juvenile

\Congenital disease (disorder)\Inborn error of metabolism\...

\Inherited metabolic disorder of nervous system\Gangliosidosis\GM2 gangliosidosis (disorder)\...

\Sandhoff disease\Total hexosaminidase deficiency - juvenile

\Juvenile GM2 gangliosidosis (disorder)\Total hexosaminidase deficiency - juvenile

\Storage disease\Disorder of lysosomal enzyme\Gangliosidosis\GM2 gangliosidosis (disorder)\...

\Sandhoff disease\Total hexosaminidase deficiency - juvenile

\Juvenile GM2 gangliosidosis (disorder)\Total hexosaminidase deficiency - juvenile

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

356756013 Total hexosaminidase deficiency - juvenile en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

626839018 Total hexosaminidase deficiency - juvenile (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

792851000052110 juvenil total hexosaminidasbrist 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
Total hexosaminidase deficiency - juvenile	Is a	Sandhoff disease	true	Inferred relationship	Some
Total hexosaminidase deficiency - juvenile	Is a	Juvenile GM2 gangliosidosis (disorder)	true	Inferred relationship	Some
Total hexosaminidase deficiency - juvenile	Occurrence	Congenital	true	Inferred relationship	Some	3
Total hexosaminidase deficiency - juvenile	Finding site	Structure of nervous system (body structure)	true	Inferred relationship	Some	1
Total hexosaminidase deficiency - juvenile	Occurrence	Childhood	true	Inferred relationship	Some	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

GB English

US English

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
356756013	Total hexosaminidase deficiency - juvenile	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
626839018	Total hexosaminidase deficiency - juvenile (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
792851000052110	juvenil total hexosaminidasbrist	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)