236470002: Specific renal tubule transport defect (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

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

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

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

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

Descriptions:

Expanded Value Set

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

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
High renal threshold for glucose	Is a	True	Specific renal tubule transport defect (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Isolated hypercystinuria	Is a	True	Specific renal tubule transport defect (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Dibasic aminoaciduria	Is a	True	Specific renal tubule transport defect (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Glycinuria	Is a	True	Specific renal tubule transport defect (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial renal hypouricaemia	Is a	True	Specific renal tubule transport defect (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Renal glycosuria	Is a	True	Specific renal tubule transport defect (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial methionine malabsorption	Is a	True	Specific renal tubule transport defect (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Histidine transport defect (disorder)	Is a	True	Specific renal tubule transport defect (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Neutral 1 amino acid transport defect	Is a	True	Specific renal tubule transport defect (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial hypokalemic alkalosis, Gullner type (disorder)	Is a	True	Specific renal tubule transport defect (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial x-linked hypophosphatemic vitamin D refractory rickets	Is a	False	Specific renal tubule transport defect (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Iminoglycinuria	Is a	True	Specific renal tubule transport defect (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Cystinuria (disorder)	Is a	True	Specific renal tubule transport defect (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Autosomal dominant hypophosphatemic bone disease	Is a	False	Specific renal tubule transport defect (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Hypophosphatemic rickets with nephrotic-glycosuric dwarfism	Due to	True	Specific renal tubule transport defect (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Autosomal dominant hypophosphatemic bone disease	Due to	False	Specific renal tubule transport defect (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Autosomal dominant hypophosphatemic rickets	Due to	False	Specific renal tubule transport defect (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Familial x-linked hypophosphatemic vitamin D refractory rickets	Due to	True	Specific renal tubule transport defect (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis	Due to	False	Specific renal tubule transport defect (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Autosomal dominant hypophosphatemic rickets	Due to	True	Specific renal tubule transport defect (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Autosomal dominant hypophosphatemic bone disease	Due to	True	Specific renal tubule transport defect (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis	Due to	True	Specific renal tubule transport defect (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)	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 (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
625067018	Specific renal tubule transport defect (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
354470014	Specific renal tubule transport defect	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
354470014	Specific renal tubule transport defect	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
625067018	Specific renal tubule transport defect (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
625067018	Specific renal tubule transport defect (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core