SNOMED CT code SNOMED code 48130008 name Hypogonadism status active date introduced 2002-01-31 fully specified name(s) Hypogonadism (disorder) synonyms Hypogonadism attributes - group1 Finding site Gonadal endocrine structure 304041004 parents Disorder of endocrine gonad 127345001 children Boucher Neuhäuser syndrome 715984007 Congenital cataract with deafness and hypogonadism syndrome 722378009 Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome 715429006 Deafness and hypogonadism syndrome 718714006 Female hypogonadism syndrome 16041008 Frontonasal dysplasia with alopecia and genital anomaly syndrome 725029001 Gonad postablative failure 286918006 Hypogonadal obesity 5036006 Hypogonadotropic hypogonadism 33927004 Infantilism 59892004 Male hypogonadism 48723006 Primary hypogonadism 370999003 Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome 724001005 Scholte syndrome 722002002 Syndromic X-linked intellectual disability type 7 719160009 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 Clinical finding 404684003 Finding by site 118234003 Disorder by body site 123946008 Disorder of body system 362965005 Disorder of endocrine system 362969004 Disorder of endocrine gonad 127345001 Hypogonadism 48130008 ancestors sorted most to least specific
cpt crosswalks Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts. Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.
Access to this feature is available in the following products:CPT® to SNOMED Crosswalks sign IN sign UP
Thank you for choosing Find-A-Code, please Sign In to remove ads.