Hypogonadotropic hypogonadism retinitis pigmentosa syndrome 733113002
SNOMED CT code
SNOMED code | 733113002 |
---|---|
name | Hypogonadotropic hypogonadism retinitis pigmentosa syndrome |
status | active |
date introduced | 2017-07-31 |
fully specified name(s) | Hypogonadotropic hypogonadism retinitis pigmentosa syndrome (disorder) |
synonyms |
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attributes - group3 | |
Associated morphology | Dystrophy 4720007 |
Occurrence | Congenital 255399007 |
Finding site | Retinal structure 5665001 |
attributes - group4 | |
Occurrence | Congenital 255399007 |
Finding site | Gonadal endocrine structure 304041004 |
attributes - group5 | |
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 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Hereditary retinal dystrophy 41799005 Retinitis pigmentosa 28835009 Hypogonadotropic hypogonadism retinitis pigmentosa syndrome 733113002 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 Hypogonadotropic hypogonadism retinitis pigmentosa syndrome 733113002 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 Hypogonadotropic hypogonadism retinitis pigmentosa syndrome 733113002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Hereditary disorder by system 363137000 Reproductive system hereditary disorder 363290007 Hypogonadotropic hypogonadism retinitis pigmentosa syndrome 733113002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital hypogonadotropic hypogonadism 722944006 Hypogonadotropic hypogonadism retinitis pigmentosa syndrome 733113002 |
ancestors | sorted most to least specific
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cpt crosswalks |
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