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68616007: Primary atrophy (morphologic abnormality)

SNOMED CT Concept\Body structure\Morphologically altered structure\Morphologically abnormal structure (morphologic abnormality)\Degenerative abnormality (morphologic abnormality)\Atrophy\Primary atrophy

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Primary atrophy	Is a	Atrophy	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hereditary motor and sensory neuropathy with optic atrophy	Associated morphology	False	Primary atrophy	Inferred relationship	Some	1
Primary lacrimal atrophy	Associated morphology	False	Primary atrophy	Inferred relationship	Some	1
Dominant hereditary optic atrophy	Associated morphology	False	Primary atrophy	Inferred relationship	Some	1
Primary optic atrophy	Associated morphology	False	Primary atrophy	Inferred relationship	Some	1
Hereditary optic atrophy	Associated morphology	False	Primary atrophy	Inferred relationship	Some	1
Leber's optic atrophy	Associated morphology	False	Primary atrophy	Inferred relationship	Some	1
Hereditary optic atrophy NOS	Associated morphology	False	Primary atrophy	Inferred relationship	Some	1
Leber's optic atrophy	Associated morphology	True	Primary atrophy	Inferred relationship	Some	1
Hereditary motor and sensory neuropathy with optic atrophy	Associated morphology	True	Primary atrophy	Inferred relationship	Some	1
Primary optic atrophy	Associated morphology	True	Primary atrophy	Inferred relationship	Some	1
Dominant hereditary optic atrophy	Associated morphology	True	Primary atrophy	Inferred relationship	Some	1
Primary lacrimal atrophy	Associated morphology	True	Primary atrophy	Inferred relationship	Some	1
Hereditary optic atrophy NOS	Associated morphology	False	Primary atrophy	Inferred relationship	Some	1
Hereditary optic atrophy	Associated morphology	True	Primary atrophy	Inferred relationship	Some	1
Autosomal dominant optic atrophy plus syndrome (disorder)	Associated morphology	True	Primary atrophy	Inferred relationship	Some	1
Autosomal dominant optic atrophy classic form (disorder)	Associated morphology	True	Primary atrophy	Inferred relationship	Some	1
Autosomal dominant optic atrophy and peripheral neuropathy syndrome (disorder)	Associated morphology	True	Primary atrophy	Inferred relationship	Some	2
Leber plus disease (disorder)	Associated morphology	True	Primary atrophy	Inferred relationship	Some	2
Autosomal dominant optic atrophy and cataract (disorder)	Associated morphology	True	Primary atrophy	Inferred relationship	Some	2
Early-onset X-linked optic atrophy (disorder)	Associated morphology	True	Primary atrophy	Inferred relationship	Some	2
Hereditary bilateral optic atrophy (disorder)	Associated morphology	True	Primary atrophy	Inferred relationship	Some	3
Hereditary bilateral optic atrophy (disorder)	Associated morphology	True	Primary atrophy	Inferred relationship	Some	4
Hereditary right optic atrophy (disorder)	Associated morphology	True	Primary atrophy	Inferred relationship	Some	2
Hereditary left optic atrophy (disorder)	Associated morphology	True	Primary atrophy	Inferred relationship	Some	2
Spastic paraplegia, optic atrophy, neuropathy syndrome (disorder)	Associated morphology	False	Primary atrophy	Inferred relationship	Some	6
Wolfram-like syndrome (disorder)	Associated morphology	True	Primary atrophy	Inferred relationship	Some	7
Optic atrophy, intellectual disability syndrome (disorder)	Associated morphology	True	Primary atrophy	Inferred relationship	Some	1
Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome (disorder)	Associated morphology	True	Primary atrophy	Inferred relationship	Some	1
Infantile cerebellar and retinal degeneration (disorder)	Associated morphology	True	Primary atrophy	Inferred relationship	Some	3
Autosomal recessive optic atrophy type 7 (disorder)	Associated morphology	True	Primary atrophy	Inferred relationship	Some	1
Arts syndrome	Associated morphology	True	Primary atrophy	Inferred relationship	Some	1
Autosomal recessive spastic paraplegia type 55 (disorder)	Associated morphology	False	Primary atrophy	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 57 (disorder)	Associated morphology	False	Primary atrophy	Inferred relationship	Some	3
SPOAN and SPOAN-related disorder	Associated morphology	True	Primary atrophy	Inferred relationship	Some	2
Autosomal recessive optic atrophy type 6	Associated morphology	True	Primary atrophy	Inferred relationship	Some	1
Childhood-onset autosomal dominant optic atrophy	Associated morphology	True	Primary atrophy	Inferred relationship	Some	1
Primary optic atrophy of bilateral eyes (disorder)	Associated morphology	True	Primary atrophy	Inferred relationship	Some	1
Primary optic atrophy of bilateral eyes (disorder)	Associated morphology	True	Primary atrophy	Inferred relationship	Some	2
Autosomal recessive bilateral optic atrophy (disorder)	Associated morphology	True	Primary atrophy	Inferred relationship	Some	1
Autosomal recessive bilateral optic atrophy (disorder)	Associated morphology	True	Primary atrophy	Inferred relationship	Some	2
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome (disorder)	Associated morphology	True	Primary atrophy	Inferred relationship	Some	2
Autosomal recessive spastic paraplegia type 74	Associated morphology	True	Primary atrophy	Inferred relationship	Some	2
Autosomal recessive spastic paraplegia type 55 (disorder)	Associated morphology	True	Primary atrophy	Inferred relationship	Some	2
Autosomal recessive spastic paraplegia type 57 (disorder)	Associated morphology	True	Primary atrophy	Inferred relationship	Some	2
Spastic paraplegia, optic atrophy, neuropathy syndrome (disorder)	Associated morphology	True	Primary atrophy	Inferred relationship	Some	2
X-linked optic atrophy	Associated morphology	True	Primary atrophy	Inferred relationship	Some	1
Mitochondrial enoyl coenzyme A reductase protein-associated neurodegeneration syndrome (disorder)	Associated morphology	True	Primary atrophy	Inferred relationship	Some	1
Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome (disorder)	Associated morphology	True	Primary atrophy	Inferred relationship	Some	1

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
113973012	Primary atrophy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
113974018	Essential atrophy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
808471016	Primary atrophy (morphologic abnormality)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4061000052113	primär atrofi	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)