Prader-Willi-like syndrome 770680004
SNOMED CT code
SNOMED code | 770680004 |
---|---|
name | Prader-Willi-like syndrome |
status | active |
date introduced | 2019-01-31 |
fully specified name(s) | Prader-Willi-like syndrome (disorder) |
synonyms | Prader-Willi-like syndrome |
attributes - group1 | |
Associated morphology | Morphologically abnormal structure 49755003 |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Finding site | Face structure 89545001 |
attributes - group3 | |
Pathological process | Pathological developmental process 308490002 |
Finding site | Gonadal endocrine structure 304041004 |
Occurrence | Congenital 255399007 |
attributes - group2 | |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Finding site | Structure of distal part of pituitary 52618001 |
attributes - group4 | |
Has interpretation | Above reference range 281302008 |
Interprets | Body weight measure 363808001 |
parents | |
children |
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hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Obesity 414916001 Prader-Willi-like syndrome 770680004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Multiple malformation syndrome with unusual brain and/or neuromuscular findings 64162006 Prader-Willi-like syndrome 770680004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of head 118934005 Disorder of face 118930001 Congenital anomaly of face 398302004 Multiple malformation syndrome with facial defects as major feature 65094009 Prader-Willi-like syndrome 770680004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital hypogonadotropic hypogonadism 722944006 Prader-Willi-like syndrome 770680004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Prader-Willi-like syndrome 770680004 |
ancestors | sorted most to least specific
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cpt crosswalks |
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