Autosomal dominant optic atrophy plus syndrome 715374003

SNOMED CT code

SNOMED code

715374003

name

Autosomal dominant optic atrophy plus syndrome

status

active

date introduced

2016-07-31

fully specified name(s)

Autosomal dominant optic atrophy plus syndrome (disorder)

synonyms

Autosomal dominant optic atrophy plus syndrome
ADOA (autosomal dominant optic atrophy) plus

attributes - group1

Associated morphology

Primary atrophy 68616007

Finding site

Optic nerve structure 18234004

parents

Dominant hereditary optic atrophy 2065009
Mitochondrial cytopathy 240096000

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Autosomal dominant hereditary disorder 11164009
Dominant hereditary optic atrophy 2065009
Autosomal dominant optic atrophy plus syndrome 715374003

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Metabolic disease 75934005
Mitochondrial cytopathy 240096000
Autosomal dominant optic atrophy plus syndrome 715374003

ancestors

sorted most to least specific

Dominant hereditary optic atrophy 2065009
Mitochondrial cytopathy 240096000
Autosomal dominant hereditary disorder 11164009
Metabolic disease 75934005
Hereditary optic atrophy 26360005
Autosomal hereditary disorder 1899006
Hereditary degenerative disease of central nervous system 106018006
Primary optic atrophy 21098003
Inherited optic neuropathy 312942003
Hereditary disorder of nervous system 363235000
Optic atrophy 76976005
Hereditary disorder of the visual system 363343008
Disorder of optic nerve 77157004
Degenerative disease of the central nervous system 80690008
Hereditary disorder by system 363137000
Hereditary disease 32895009
Disorder of visual pathways 54767005
Cranial nerve disorder 73013002
Degenerative disorder 362975008
Genetic disease 782964007
Visual system disorder 128127008
Disorder of the central nervous system 23853001
Neuropathy 386033004
Disorder of nervous system 118940003
Eye / vision finding 118235002
Central nervous system finding 246556002
Disorder of body system 362965005
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

cpt crosswalks

Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts. Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.

Access to this feature is available in the following products:

CPT® to SNOMED Crosswalks

Thank you for choosing Find-A-Code, please Sign In to remove ads.

MY NEWSLETTERS

FEES

FACILITY

RISK ADJUSTMENT

SNOMED CT Concept 138875005

Clinical finding 404684003

Disease 64572001

Genetic disease 782964007

Hereditary disease 32895009

Autosomal hereditary disorder 1899006

Autosomal dominant hereditary disorder 11164009

Dominant hereditary optic atrophy 2065009

Autosomal dominant optic atrophy plus syndrome 715374003

SNOMED CT code