FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

68616007: Primary atrophy (morphologic abnormality)

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
113973012 Primary atrophy en Synonym Active Entire term case insensitive SNOMED CT core module
113974018 Essential atrophy en Synonym Active Entire term case insensitive SNOMED CT core module
808471016 Primary atrophy (morphologic abnormality) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

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

This concept is not in any reference sets

Back to Start