236470002: Specific renal tubule transport defect (disorder)

SNOMED CT Concept\Clinical finding\...

\Viscus structure finding\Abdominal organ finding\Kidney finding\Kidney disease\Specific renal tubule transport defect

\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneal compartment\Kidney disease\Specific renal tubule transport defect
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system\Disorder of the urinary system\Disorder of kidney and/or ureter\Kidney disease\Specific renal tubule transport defect
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Kidney finding\Kidney disease\Specific renal tubule transport defect
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Disorder of retroperitoneal compartment\Kidney disease\Specific renal tubule transport defect
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Urogenital finding\Urinary system finding\Kidney finding\Kidney disease\Specific renal tubule transport defect
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Urogenital finding\Urinary system finding\Disorder of the urinary system\Disorder of kidney and/or ureter\Kidney disease\Specific renal tubule transport defect
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Urogenital finding\Disorder of the genitourinary system\Disorder of the urinary system\Disorder of kidney and/or ureter\Kidney disease\Specific renal tubule transport defect
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneal compartment\Kidney disease\Specific renal tubule transport defect
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system\Disorder of the urinary system\Disorder of kidney and/or ureter\Kidney disease\Specific renal tubule transport defect

\Disease\Disorder of body system\Disorder of the genitourinary system\Disorder of the urinary system\Disorder of kidney and/or ureter\Kidney disease\Specific renal tubule transport defect
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneal compartment\Kidney disease\Specific renal tubule transport defect
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system\Disorder of the urinary system\Disorder of kidney and/or ureter\Kidney disease\Specific renal tubule transport defect

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

354470014 Specific renal tubule transport defect en Synonym Active Entire term case insensitive SNOMED CT core module

625067018 Specific renal tubule transport defect (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Specific renal tubule transport defect	Is a	Structural and functional abnormalities of the kidney	false	Inferred relationship	Existential restriction modifier
Specific renal tubule transport defect	Finding site	Kidney structure	true	Inferred relationship	Existential restriction modifier	1
Specific renal tubule transport defect	Is a	Kidney disease	true	Inferred relationship	Existential restriction modifier

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
High renal threshold for glucose	Is a	True	Specific renal tubule transport defect	Inferred relationship	Existential restriction modifier
Isolated hypercystinuria	Is a	True	Specific renal tubule transport defect	Inferred relationship	Existential restriction modifier
Dibasic aminoaciduria	Is a	True	Specific renal tubule transport defect	Inferred relationship	Existential restriction modifier
Glycinuria	Is a	True	Specific renal tubule transport defect	Inferred relationship	Existential restriction modifier
Familial renal hypouricemia	Is a	True	Specific renal tubule transport defect	Inferred relationship	Existential restriction modifier
Renal glycosuria	Is a	True	Specific renal tubule transport defect	Inferred relationship	Existential restriction modifier
Familial methionine malabsorption	Is a	True	Specific renal tubule transport defect	Inferred relationship	Existential restriction modifier
Histidine transport defect	Is a	True	Specific renal tubule transport defect	Inferred relationship	Existential restriction modifier
Neutral 1 amino acid transport defect	Is a	True	Specific renal tubule transport defect	Inferred relationship	Existential restriction modifier
Familial hypokalemic alkalosis, Gullner type	Is a	True	Specific renal tubule transport defect	Inferred relationship	Existential restriction modifier
Familial x-linked hypophosphatemic vitamin D refractory rickets	Is a	False	Specific renal tubule transport defect	Inferred relationship	Existential restriction modifier
Iminoglycinuria	Is a	True	Specific renal tubule transport defect	Inferred relationship	Existential restriction modifier
Cystinuria	Is a	True	Specific renal tubule transport defect	Inferred relationship	Existential restriction modifier
Autosomal dominant hypophosphatemic bone disease	Is a	False	Specific renal tubule transport defect	Inferred relationship	Existential restriction modifier
Hypophosphatemic rickets with nephrotic-glycosuric dwarfism	Due to	True	Specific renal tubule transport defect	Inferred relationship	Existential restriction modifier	1
Autosomal dominant hypophosphatemic bone disease	Due to	False	Specific renal tubule transport defect	Inferred relationship	Existential restriction modifier	2
Autosomal dominant hypophosphatemic rickets	Due to	False	Specific renal tubule transport defect	Inferred relationship	Existential restriction modifier	2
Familial x-linked hypophosphatemic vitamin D refractory rickets	Due to	True	Specific renal tubule transport defect	Inferred relationship	Existential restriction modifier	2
Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis	Due to	False	Specific renal tubule transport defect	Inferred relationship	Existential restriction modifier	3
Autosomal dominant hypophosphatemic rickets	Due to	True	Specific renal tubule transport defect	Inferred relationship	Existential restriction modifier	3
Autosomal dominant hypophosphatemic bone disease	Due to	True	Specific renal tubule transport defect	Inferred relationship	Existential restriction modifier	3
Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis	Due to	True	Specific renal tubule transport defect	Inferred relationship	Existential restriction modifier	4

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
354470014	Specific renal tubule transport defect	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
625067018	Specific renal tubule transport defect (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module