Oculogastrointestinal muscular dystrophy 722060007

SNOMED CT code

SNOMED code

722060007

name

Oculogastrointestinal muscular dystrophy

status

active

date introduced

2017-01-31

fully specified name(s)

Oculogastrointestinal muscular dystrophy (disorder)

synonyms

Oculogastrointestinal muscular dystrophy
Visceral myopathy with familial external ophthalmoplegia syndrome

attributes - group1

Finding site

Visual structure 49549006

Occurrence

Congenital 255399007

Associated morphology

Morphologically abnormal structure 49755003

Pathological process

Pathological developmental process 308490002

attributes - group2

Pathological process

Pathological developmental process 308490002

Associated morphology

Pseudo-obstruction 27266007

Occurrence

Congenital 255399007

Finding site

Intestinal structure 113276009

parents

Congenital anomaly of intestinal tract 126764002
Congenital anomaly of visual system 127329003
Pseudo-obstruction of intestine 235825006
Developmental hereditary disorder 363070008
Digestive system hereditary disorder 363080007
Hereditary disorder of the visual system 363343008
Autosomal recessive hereditary disorder 85995004

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Viscus structure finding 406123005
Abdominal organ finding 249561001
Bowel finding 249562008
Disorder of intestine 85919009
Congenital anomaly of intestinal tract 126764002
Oculogastrointestinal muscular dystrophy 722060007

SNOMED CT Concept 138875005
Clinical finding 404684003
Eye / vision finding 118235002
Visual system disorder 128127008
Congenital anomaly of visual system 127329003
Oculogastrointestinal muscular dystrophy 722060007

SNOMED CT Concept 138875005
Clinical finding 404684003
Digestive system finding 386617003
Gastrointestinal tract finding 386618008
Disorder of gastrointestinal tract 119292006
Pseudo-obstruction of gastrointestinal tract 197056004
Pseudo-obstruction of intestine 235825006
Oculogastrointestinal muscular dystrophy 722060007

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Developmental hereditary disorder 363070008
Oculogastrointestinal muscular dystrophy 722060007

SNOMED CT Concept 138875005
Clinical finding 404684003
Digestive system finding 386617003
Disorder of digestive system 53619000
Digestive system hereditary disorder 363080007
Oculogastrointestinal muscular dystrophy 722060007

SNOMED CT Concept 138875005
Clinical finding 404684003
Eye / vision finding 118235002
Visual system disorder 128127008
Hereditary disorder of the visual system 363343008
Oculogastrointestinal muscular dystrophy 722060007

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Autosomal recessive hereditary disorder 85995004
Oculogastrointestinal muscular dystrophy 722060007

ancestors

sorted most to least specific

Congenital anomaly of intestinal tract 126764002
Congenital anomaly of visual system 127329003
Pseudo-obstruction of intestine 235825006
Developmental hereditary disorder 363070008
Digestive system hereditary disorder 363080007
Hereditary disorder of the visual system 363343008
Autosomal recessive hereditary disorder 85995004
Congenital anomaly of digestive organ 128332003
Visual system disorder 128127008
Pseudo-obstruction of gastrointestinal tract 197056004
Hereditary disorder by system 363137000
Autosomal hereditary disorder 1899006
Congenital anomaly of lower alimentary tract 31686000
Motility disorder of intestine 235823004
Eye / vision finding 118235002
Hereditary disease 32895009
Congenital anomaly of gastrointestinal tract 128347007
Functional disorder of intestine 81120009
Congenital anomaly of abdomen 363024001
Genetic disease 782964007
Disorder of intestine 85919009
Congenital anomaly of digestive tract 95470009
Congenital anomaly of lower trunk 363030001
Congenital anomaly of digestive system 69518005
Bowel finding 249562008
Disorder of digestive organ 76712006
Disorder of lower gastrointestinal tract 79787007
Congenital abnormality of lower limb and pelvic girdle 253937004
Congenital anomaly of trunk 78626001
Congenital malformation 276654001
Disorder of gastrointestinal tract 119292006
Abdominal organ finding 249561001
Disorder of abdomen 118948005
Developmental disorder 5294002
Gastrointestinal tract finding 386618008
Viscus structure finding 406123005
Congenital disease 66091009
Disorder of digestive tract 84410009
Finding of abdomen 609624008
Disorder of abdominopelvic segment of trunk 822988000
Disorder of digestive system 53619000
Finding of abdominopelvic segment of trunk 822987005
Disorder of trunk 128121009
Digestive system finding 386617003
Disorder of body system 362965005
Finding of trunk structure 302292003
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

Viscus structure finding 406123005

Abdominal organ finding 249561001

Bowel finding 249562008

Disorder of intestine 85919009

Congenital anomaly of intestinal tract 126764002

Oculogastrointestinal muscular dystrophy 722060007

SNOMED CT code