46,XX ovarian dysgenesis, short stature syndrome 1237345002
SNOMED CT code
| SNOMED code | 1237345002 |
|---|---|
| name | 46,XX ovarian dysgenesis, short stature syndrome |
| status | active |
| date introduced | 2022-09-30 |
| fully specified name(s) | 46,XX ovarian dysgenesis, short stature syndrome (disorder) |
| synonyms | 46,XX ovarian dysgenesis, short stature syndrome |
| attributes - group2 | |
| Interprets | Hormone secretion 60877009 |
| Has interpretation | Decreased 1250004 |
| attributes - group3 | |
| Interprets | Body height measure 50373000 |
| Has interpretation | Below reference range 281300000 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Ovarian endocrine structure 304043001 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Endocrine finding 106176003 Decreased hormone secretion 42497006 Ovarian failure 111550004 Primary ovarian failure 65846009 Ovarian dysgenesis 205683001 46,XX ovarian dysgenesis, short stature syndrome 1237345002 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of general physiological development 271616002 Disorder of stature 237834000 Short stature disorder 237836003 46,XX ovarian dysgenesis, short stature syndrome 1237345002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 46,XX ovarian dysgenesis, short stature syndrome 1237345002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Hereditary disorder of endocrine system 363104002 46,XX ovarian dysgenesis, short stature syndrome 1237345002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Hereditary disorder by system 363137000 Reproductive system hereditary disorder 363290007 46,XX ovarian dysgenesis, short stature syndrome 1237345002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 46,XX ovarian dysgenesis, short stature syndrome 1237345002 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of trunk structure 302292003 Finding of abdominopelvic segment of trunk 822987005 Urogenital finding 118238000 Genital finding 300479008 Congenital malformation of genital organs 204821009 46,XX disorder of sex development 890460004 46,XX ovarian dysgenesis, short stature syndrome 1237345002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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