Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome 773647007
SNOMED CT code
SNOMED code | 773647007 |
---|---|
name | Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome |
status | active |
date introduced | 2019-01-31 |
fully specified name(s) | Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome (disorder) |
synonyms |
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attributes - group1 | |
Finding site | Glomerulus structure 68288006 |
Associated morphology | Chronic inflammatory morphology 409777003 |
attributes - group4 | |
Finding site | Ear structure 117590005 |
attributes - group5 | |
Interprets | Hearing 47078008 |
attributes - group3 | |
Has interpretation | Below reference range 281300000 |
Interprets | Albumin measurement 26758005 |
attributes - group2 | |
Has interpretation | Above reference range 281302008 |
Interprets | Urine protein measurement 57378007 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Functional finding 118228005 Hearing finding 118230007 Hearing disorder 128540005 Hearing loss 15188001 Hearing loss associated with syndrome 232333009 Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome 773647007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of sensory organ 1279550006 Disorder of ear 25906001 Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome 773647007 SNOMED CT Concept 138875005 Clinical finding 404684003 Ear and auditory finding 118236001 Disorder of auditory system 362966006 Auditory system hereditary disorder 362991006 Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome 773647007 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Kidney finding 249578005 Kidney disease 90708001 Hereditary nephropathy 367591000119105 Hereditary nephritis 399340005 Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome 773647007 SNOMED CT Concept 138875005 Clinical finding 404684003 Urine finding 301830001 Finding of urine substance level 785672002 Urine substance level above reference range 1217345006 Proteinuria 29738008 Protein-losing nephropathy 370494002 Nephrotic syndrome 52254009 Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome 773647007 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Hearing finding 118230007 Hearing disorder 128540005 Hearing loss 15188001 Sensorineural hearing loss 60700002 Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome 773647007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome 773647007 |
ancestors | sorted most to least specific
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cpt crosswalks |
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