Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies 774152007

SNOMED CT code

SNOMED code

774152007

name

Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies

status

active

date introduced

2019-01-31

fully specified name(s)

Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies (disorder)

synonyms

Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies
Retinal dystrophy with inner nuclear layer and ganglion cell anomalies

attributes - group1

Finding site

Retinal structure 5665001

Associated morphology

Dystrophy 4720007

parents

Autosomal dominant hereditary disorder 11164009
Hereditary retinal dystrophy 41799005

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
Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies 774152007

SNOMED CT Concept 138875005
Clinical finding 404684003
Eye / vision finding 118235002
Visual system disorder 128127008
Hereditary disorder of the visual system 363343008
Hereditary retinal dystrophy 41799005
Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies 774152007

ancestors

sorted most to least specific

Autosomal dominant hereditary disorder 11164009
Hereditary retinal dystrophy 41799005
Autosomal hereditary disorder 1899006
Retinal dystrophy 314407005
Hereditary disorder of the visual system 363343008
Degeneration of retina 95695004
Hereditary disorder by system 363137000
Hereditary disease 32895009
Retinal disorder 29555009
Degenerative disorder of eye 62585004
Genetic disease 782964007
Disorder of vitreous body and retina 312771007
Anomaly of eye 11131000119108
Retina finding 399858007
Degenerative disorder 362975008
Disorder of posterior segment of eye 128536001
Disorder of eye 371405004
Disorder of sensory organ 1279550006
Globe finding 246915008
Disorder of eye region 371409005
Visual system disorder 128127008
Disorder of head 118934005
Finding of head region 298364001
Eye / vision finding 118235002
Head finding 406122000
Disorder of body system 362965005
Disease 64572001
Finding of head and neck region 118254002
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

Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies 774152007

SNOMED CT code