Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement 717787005

SNOMED CT code

SNOMED code

717787005

name

Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement

status

active

date introduced

2017-01-31

fully specified name(s)

Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement (disorder)

synonyms

Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement
Familial hypomagnesaemia hypercalciuria nephrocalcinosis with severe ocular involvement

attributes - group1

Finding site

Urinary system structure 122489005

parents

Hereditary disorder of the urinary system 363338001
Familial hypomagnesemia-hypercalciuria 50029007
Autosomal recessive hereditary disorder 85995004

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Disorder of body system 362965005
Hereditary disorder by system 363137000
Hereditary disorder of the urinary system 363338001
Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement 717787005

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Metabolic disease 75934005
Metabolic disorder of transport 111394006
Primary hypomagnesemia 80710001
Familial hypomagnesemia-hypercalciuria 50029007
Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement 717787005

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Autosomal recessive hereditary disorder 85995004
Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement 717787005

ancestors

sorted most to least specific

Hereditary disorder of the urinary system 363338001
Familial hypomagnesemia-hypercalciuria 50029007
Autosomal recessive hereditary disorder 85995004
Hypercalciuria 71938000
Autosomal hereditary disorder 1899006
Hereditary disorder by system 363137000
Primary hypomagnesemia 80710001
Symptomatic disorders of the urinary tract 236714000
Hereditary disease 32895009
Metabolic disorder of transport 111394006
Disorder of calcium metabolism 71638002
Hypomagnesemia 190855004
Disorder of the urinary system 128606002
Genetic disease 782964007
Disorder of phosphate, calcium and vitamin D metabolism 237879001
Magnesium disorder 420200001
Urinary system finding 106098005
Disorder of the genitourinary system 42030000
Disorder of mineral metabolism 45744005
Disorder of electrolytes 237840007
Urogenital finding 118238000
Disorder of body system 362965005
Disorder of abdominopelvic segment of trunk 822988000
Disorder of fluid AND/OR electrolyte 76314005
Finding of abdominopelvic segment of trunk 822987005
Metabolic disease 75934005
Disorder of trunk 128121009
Finding of trunk structure 302292003
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

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

Thank you for choosing Find-A-Code, please Sign In to remove ads.

MY NEWSLETTERS

FEES

FACILITY

RISK ADJUSTMENT

SNOMED CT Concept 138875005

Clinical finding 404684003

Disease 64572001

Disorder of body system 362965005

Hereditary disorder by system 363137000

Hereditary disorder of the urinary system 363338001

Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement 717787005

SNOMED CT code