Achalasia microcephaly syndrome 718573009
SNOMED CT code
| SNOMED code | 718573009 |
|---|---|
| name | Achalasia microcephaly syndrome |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Achalasia microcephaly syndrome (disorder) |
| synonyms | Achalasia microcephaly syndrome |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Head structure 69536005 |
| Associated morphology | Congenital smallness 41086002 |
| attributes - group4 | |
| Has interpretation | Below reference range 281300000 |
| Interprets | Birth head circumference 169876006 |
| attributes - group5 | |
| Interprets | Intellectual ability 247573007 |
| Has interpretation | Impaired 260379002 |
| attributes - group6 | |
| Interprets | Adaptation behavior 406208005 |
| Has interpretation | Impaired 260379002 |
| attributes - group3 | |
| Occurrence | Congenital 255399007 |
| Finding site | Cardioesophageal junction structure 25271004 |
| attributes - group1 | |
| Has interpretation | Abnormal 263654008 |
| Interprets | Motility 398598008 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Mental state, behavior and/or psychosocial function finding 384821006 Behavior finding 844005 Intellectual disability 110359009 Achalasia microcephaly syndrome 718573009 SNOMED CT Concept 138875005 Clinical finding 404684003 Body measurement finding 365605003 Finding of head circumference 301338002 Microcephaly 1148757008 Congenital microcephaly 1148758003 Achalasia microcephaly syndrome 718573009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Achalasia microcephaly syndrome 718573009 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Achalasia microcephaly syndrome 718573009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital achalasia of esophagus 700283004 Achalasia microcephaly syndrome 718573009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Achalasia microcephaly syndrome 718573009 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
Thank you for choosing Find-A-Code, please Sign In to remove ads.
Quick, Current, Complete - www.findacode.com