Bartter syndrome type 4 700112007

SNOMED CT code

SNOMED code

700112007

name

Bartter syndrome type 4

status

active

date introduced

2014-07-31

fully specified name(s)

Bartter syndrome type 4 (disorder)

synonyms

Bartter syndrome type 4
Bartter's syndrome type 4

attributes - group1

Has interpretation

Impaired 260379002

Interprets

Tubular sodium chloride reabsorption function 840727000

attributes - group2

Finding site

Auditory structure 91159003

Occurrence

Congenital 255399007

attributes - group3

Finding site

Structure of medullary thick ascending limb of loop of Henle 840723001

attributes - group4

Interprets

Hearing 47078008

parents

Auditory system hereditary disorder 362991006
Congenital sensorineural hearing loss 700453005
Bartter syndrome 707742001

children

Bartter syndrome type 4a 717791000

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Ear and auditory finding 118236001
Disorder of auditory system 362966006
Auditory system hereditary disorder 362991006
Bartter syndrome type 4 700112007

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Congenital disease 66091009
Congenital hearing disorder 95827002
Congenital sensorineural hearing loss 700453005
Bartter syndrome type 4 700112007

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Metabolic disease 75934005
Metabolic renal disease 106000008
Bartter syndrome 707742001
Bartter syndrome type 4 700112007

ancestors

sorted most to least specific

Auditory system hereditary disorder 362991006
Congenital sensorineural hearing loss 700453005
Bartter syndrome 707742001
Sensorineural hearing loss 60700002
Metabolic renal disease 106000008
Congenital hearing disorder 95827002
Hypokalemic alkalosis 22774003
Renal impairment 236423003
Hereditary nephropathy 367591000119105
Hypochloremic alkalosis 70134007
Hypercalciuria 71938000
Autosomal recessive hereditary disorder 85995004
Renal tubular disorder 95568003
Hearing loss 15188001
Metabolic alkalosis 1388004
Finding of renal function 1148582006
Hereditary disorder of the urinary system 363338001
Symptomatic disorders of the urinary tract 236714000
Autosomal hereditary disorder 1899006
Disorder of renal parenchyma 767094002
Congenital disease 66091009
Hypokalemia 43339004
Impaired urinary system function 1156448003
Disorder of calcium metabolism 71638002
Hearing disorder 128540005
Hereditary disorder by system 363137000
Alkalosis 21420006
Kidney disease 90708001
Potassium disorder 24529006
Disorder of phosphate, calcium and vitamin D metabolism 237879001
Disorder of auditory system 362966006
Hearing finding 118230007
Hereditary disease 32895009
Disorder of acid-base balance 26436007
Kidney finding 249578005
Disorder of electrolytes 237840007
Disorder of mineral metabolism 45744005
Disorder of kidney and/or ureter 443820000
Disorder of retroperitoneum 734045002
Ear and auditory finding 118236001
Functional finding 118228005
Genetic disease 782964007
Disorder of the urinary system 128606002
Disorder of fluid AND/OR electrolyte 76314005
Disorder of abdomen 118948005
Abdominal organ finding 249561001
Metabolic disease 75934005
Urinary system finding 106098005
Disorder of the genitourinary system 42030000
Finding of abdomen 609624008
Viscus structure finding 406123005
Disorder of body system 362965005
Urogenital finding 118238000
Disorder of abdominopelvic segment of trunk 822988000
Finding of abdominopelvic segment of trunk 822987005
Disorder of trunk 128121009
Disease 64572001
Finding of trunk structure 302292003
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

Ear and auditory finding 118236001

Disorder of auditory system 362966006

Auditory system hereditary disorder 362991006

Bartter syndrome type 4 700112007

SNOMED CT code