MIRAGE syndrome 1234831009
SNOMED CT code
SNOMED code | 1234831009 |
---|---|
name | MIRAGE syndrome |
status | active |
date introduced | 2022-07-31 |
fully specified name(s) | Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome (disorder) |
synonyms |
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attributes - group3 | |
Due to | Disorder of endocrine system 362969004 |
attributes - group1 | |
Occurrence | Congenital 255399007 |
Finding site | Genital structure 71934003 |
Associated morphology | Morphologically abnormal structure 49755003 |
Pathological process | Pathological developmental process 308490002 |
attributes - group2 | |
Occurrence | Congenital 255399007 |
Finding site | Adrenal cortex structure 68594002 |
Associated morphology | Hypoplasia 55199003 |
Pathological process | Pathological developmental process 308490002 |
attributes - group4 | |
Interprets | Body height measure 50373000 |
Has interpretation | Below reference range 281300000 |
parents |
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hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 MIRAGE syndrome 1234831009 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Disorder of adrenal gland 30171000 Adrenogenital disorder 267395000 MIRAGE syndrome 1234831009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 MIRAGE syndrome 1234831009 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 MIRAGE syndrome 1234831009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Hereditary disorder by system 363137000 Reproductive system hereditary disorder 363290007 MIRAGE syndrome 1234831009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Short stature co-occurrent and due to endocrine disorder 368331000119100 MIRAGE syndrome 1234831009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 MIRAGE syndrome 1234831009 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,XY disorder of sex development 880094008 MIRAGE syndrome 1234831009 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Disorder of adrenal gland 30171000 Congenital anomaly of adrenal gland 60637003 Congenital hypoplasia of adrenal gland 93235007 MIRAGE syndrome 1234831009 |
ancestors | sorted most to least specific
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cpt crosswalks |
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