Congenital leptin deficiency 700150001
SNOMED CT code
| SNOMED code | 700150001 |
|---|---|
| name | Congenital leptin deficiency |
| status | active |
| date introduced | 2014-07-31 |
| fully specified name(s) | Congenital leptin deficiency (disorder) |
| synonyms |
|
| attributes - group4 | |
| Occurrence | Childhood 255398004 |
| attributes - group3 | |
| Interprets | Body weight measure 363808001 |
| Has interpretation | Above reference range 281302008 |
| attributes - group1 | |
| Finding site | Gonadal endocrine structure 304041004 |
| Occurrence | Congenital 255399007 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Finding site | Structure of distal part of pituitary 52618001 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Genetic non-syndromic obesity 1260139006 Congenital leptin deficiency 700150001 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 Congenital leptin deficiency 700150001 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 Congenital leptin deficiency 700150001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Hereditary disorder by system 363137000 Reproductive system hereditary disorder 363290007 Congenital leptin deficiency 700150001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital hypogonadotropic hypogonadism 722944006 Congenital leptin deficiency 700150001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Congenital leptin deficiency 700150001 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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