Obesity due to leptin receptor gene deficiency 785722006
SNOMED CT code
| SNOMED code | 785722006 |
|---|---|
| name | Obesity due to leptin receptor gene deficiency |
| status | active |
| date introduced | 2019-07-31 |
| fully specified name(s) | Obesity due to leptin receptor gene deficiency (disorder) |
| synonyms | Obesity due to leptin receptor gene deficiency |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Gonadal endocrine structure 304041004 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Finding site | Structure of distal part of pituitary 52618001 |
| attributes - group3 | |
| Interprets | Body weight measure 363808001 |
| Has interpretation | Above reference range 281302008 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Hereditary disorder of endocrine system 363104002 Obesity due to leptin receptor gene deficiency 785722006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Obesity due to leptin receptor gene deficiency 785722006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Hereditary disorder by system 363137000 Reproductive system hereditary disorder 363290007 Obesity due to leptin receptor gene deficiency 785722006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital hypogonadotropic hypogonadism 722944006 Obesity due to leptin receptor gene deficiency 785722006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Obesity 414916001 Severe obesity 83911000119104 Obesity due to leptin receptor gene deficiency 785722006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Obesity due to leptin receptor gene deficiency 785722006 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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