Congenital enterocyte heparan sulfate deficiency 725591002

SNOMED CT code

SNOMED code

725591002

name

Congenital enterocyte heparan sulfate deficiency

status

active

date introduced

2017-07-31

fully specified name(s)

Congenital enterocyte heparan sulfate deficiency (disorder)

synonyms

Congenital enterocyte heparan sulfate deficiency
Congenital enterocyte heparan sulphate deficiency

attributes - group1

Pathological process

Pathological developmental process 308490002

Associated morphology

Morphologically abnormal structure 49755003

Occurrence

Congenital 255399007

Finding site

Intestinal mucous membrane structure 68534000

parents

Congenital anomaly of intestinal tract 126764002
Disorder of gastrointestinal tract mucous membrane 128068002
Disorder of soft tissue of trunk 280133005

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
Congenital enterocyte heparan sulfate deficiency 725591002

SNOMED CT Concept 138875005
Clinical finding 404684003
Digestive system finding 386617003
Gastrointestinal tract finding 386618008
Disorder of gastrointestinal tract 119292006
Disorder of gastrointestinal tract mucous membrane 128068002
Congenital enterocyte heparan sulfate deficiency 725591002

SNOMED CT Concept 138875005
Clinical finding 404684003
Finding of trunk structure 302292003
Disorder of trunk 128121009
Disorder of soft tissue of trunk 280133005
Congenital enterocyte heparan sulfate deficiency 725591002

ancestors

sorted most to least specific

Congenital anomaly of intestinal tract 126764002
Disorder of gastrointestinal tract mucous membrane 128068002
Disorder of soft tissue of trunk 280133005
Congenital anomaly of digestive organ 128332003
Congenital anomaly of lower alimentary tract 31686000
Disorder of intestine 85919009
Disorder of mucous membrane 95351003
Disorder of soft tissue 19660004
Congenital anomaly of gastrointestinal tract 128347007
Bowel finding 249562008
Disorder of digestive organ 76712006
Mucosal finding 128145008
General finding of soft tissue 248402002
Congenital anomaly of abdomen 363024001
Disorder of lower gastrointestinal tract 79787007
Disorder of gastrointestinal tract 119292006
Abdominal organ finding 249561001
Skin AND/OR mucosa finding 415531008
Disorder of abdomen 118948005
Congenital anomaly of digestive tract 95470009
Congenital anomaly of lower trunk 363030001
Congenital anomaly of digestive system 69518005
Gastrointestinal tract finding 386618008
Viscus structure finding 406123005
Disorder of digestive tract 84410009
Finding of abdomen 609624008
Congenital abnormality of lower limb and pelvic girdle 253937004
Disorder of abdominopelvic segment of trunk 822988000
Congenital anomaly of trunk 78626001
Congenital malformation 276654001
Disorder of trunk 128121009
Disorder of digestive system 53619000
Finding of abdominopelvic segment of trunk 822987005
Developmental disorder 5294002
Digestive system finding 386617003
Finding of trunk structure 302292003
Disorder of body system 362965005
Congenital disease 66091009
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

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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

Congenital enterocyte heparan sulfate deficiency 725591002

SNOMED CT code