SIM1-related Prader-Willi-like syndrome 1229943004
SNOMED CT code
SNOMED code | 1229943004 |
---|---|
name | SIM1-related Prader-Willi-like syndrome |
status | active |
date introduced | 2022-05-31 |
fully specified name(s) | SIM bHLH transcription factor 1-related Prader-Willi-like syndrome (disorder) |
synonyms |
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attributes - group4 | |
Interprets | Body weight measure 363808001 |
Has interpretation | Above reference range 281302008 |
attributes - group1 | |
Occurrence | Congenital 255399007 |
Finding site | Face structure 89545001 |
Associated morphology | Morphologically abnormal structure 49755003 |
Pathological process | Pathological developmental process 308490002 |
attributes - group2 | |
Occurrence | Congenital 255399007 |
Finding site | Gonadal endocrine structure 304041004 |
Pathological process | Pathological developmental process 308490002 |
attributes - group3 | |
Occurrence | Congenital 255399007 |
Finding site | Structure of distal part of pituitary 52618001 |
Pathological process | Pathological developmental process 308490002 |
parents | Prader-Willi-like syndrome 770680004 |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Prader-Willi-like syndrome 770680004 SIM1-related Prader-Willi-like syndrome 1229943004 |
ancestors | sorted most to least specific
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cpt crosswalks |
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