Genitopalatocardiac syndrome 773749003
SNOMED CT code
| SNOMED code | 773749003 |
|---|---|
| name | Genitopalatocardiac syndrome |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | Genitopalatocardiac syndrome (disorder) |
| synonyms |
|
| attributes - group2 | |
| Associated morphology | Developmental failure of fusion 371520008 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Palatal structure 72914001 |
| Occurrence | Congenital 255399007 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Gonadal structure 43174007 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| attributes - group3 | |
| Finding site | Heart structure 80891009 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Cardiovascular finding 106063007 Cardiac finding 301095005 Heart disease 56265001 Structural disorder of heart 128599005 Congenital heart disease 13213009 Genitopalatocardiac syndrome 773749003 SNOMED CT Concept 138875005 Clinical finding 404684003 Cardiovascular finding 106063007 Disorder of cardiovascular system 49601007 Cardiovascular system hereditary disorder 363005004 Genitopalatocardiac syndrome 773749003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Genitopalatocardiac syndrome 773749003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Hereditary disorder by system 363137000 Reproductive system hereditary disorder 363290007 Genitopalatocardiac syndrome 773749003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Genitopalatocardiac syndrome 773749003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Genitopalatocardiac syndrome 773749003 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of head and neck region 118254002 Head finding 406122000 Finding of head region 298364001 Orofacial cleft 449790007 Cleft palate 87979003 Genitopalatocardiac syndrome 773749003 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 Gonadal dysgenesis 205681004 Pure gonadal dysgenesis 95219002 Pure gonadal dysgenesis 46,XY 95218005 Genitopalatocardiac syndrome 773749003 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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