765330003: Autosomal dominant polycystic kidney disease (disorder)

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

\Viscus structure finding (finding)\Abdominal organ finding\...

\Renal mass\Cyst of kidney (disorder)\Congenital cystic kidney disease\Autosomal dominant polycystic kidney disease (disorder)

\Kidney disease\Cyst of kidney (disorder)\Congenital cystic kidney disease\Autosomal dominant polycystic kidney disease (disorder)

\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Kidney disease\Cyst of kidney (disorder)\Congenital cystic kidney disease\Autosomal dominant polycystic kidney disease (disorder)
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system (disorder)\Disorder of kidney and/or ureter (disorder)\Kidney disease\Cyst of kidney (disorder)\Congenital cystic kidney disease\Autosomal dominant polycystic kidney disease (disorder)
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal mass\Retroperitoneal mass\Renal mass\Cyst of kidney (disorder)\Congenital cystic kidney disease\Autosomal dominant polycystic kidney disease (disorder)
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Renal mass\Cyst of kidney (disorder)\Congenital cystic kidney disease\Autosomal dominant polycystic kidney disease (disorder)
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Abdominal organ finding\Kidney disease\Cyst of kidney (disorder)\Congenital cystic kidney disease\Autosomal dominant polycystic kidney disease (disorder)
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Finding of abdomen\Disorder of abdomen (disorder)\Kidney disease\Cyst of kidney (disorder)\Congenital cystic kidney disease\Autosomal dominant polycystic kidney disease (disorder)
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Mass of urogenital structure\Renal mass\Cyst of kidney (disorder)\Congenital cystic kidney disease\Autosomal dominant polycystic kidney disease (disorder)
\Finding of trunk structure\Finding of abdominopelvic segment of trunk (finding)\Urogenital finding\Disorder of the genitourinary system (disorder)\Disorder of kidney and/or ureter (disorder)\Kidney disease\Cyst of kidney (disorder)\Congenital cystic kidney disease\Autosomal dominant polycystic kidney disease (disorder)
\Finding of trunk structure\Mass of trunk\Mass of urogenital structure\Renal mass\Cyst of kidney (disorder)\Congenital cystic kidney disease\Autosomal dominant polycystic kidney disease (disorder)
\Finding of trunk structure\Mass of trunk\Abdominal mass\Retroperitoneal mass\Renal mass\Cyst of kidney (disorder)\Congenital cystic kidney disease\Autosomal dominant polycystic kidney disease (disorder)
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Kidney disease\Cyst of kidney (disorder)\Congenital cystic kidney disease\Autosomal dominant polycystic kidney disease (disorder)
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system (disorder)\Disorder of kidney and/or ureter (disorder)\Kidney disease\Cyst of kidney (disorder)\Congenital cystic kidney disease\Autosomal dominant polycystic kidney disease (disorder)

\Mass of body structure\Mass of body region\Mass of trunk\...

\Mass of urogenital structure\Renal mass\Cyst of kidney (disorder)\Congenital cystic kidney disease\Autosomal dominant polycystic kidney disease (disorder)

\Abdominal mass\Retroperitoneal mass\Renal mass\Cyst of kidney (disorder)\Congenital cystic kidney disease\Autosomal dominant polycystic kidney disease (disorder)

\Disease\Genetic disease\Hereditary disease\Autosomal dominant hereditary disorder\Autosomal dominant polycystic kidney disease (disorder)
\Disease\Cyst (disorder)\Cyst of kidney (disorder)\Congenital cystic kidney disease\Autosomal dominant polycystic kidney disease (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital cystic kidney disease\Autosomal dominant polycystic kidney disease (disorder)
\Disease\Disorder of body system\Disorder of the genitourinary system (disorder)\Disorder of kidney and/or ureter (disorder)\Kidney disease\Cyst of kidney (disorder)\Congenital cystic kidney disease\Autosomal dominant polycystic kidney disease (disorder)
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of abdomen (disorder)\Kidney disease\Cyst of kidney (disorder)\Congenital cystic kidney disease\Autosomal dominant polycystic kidney disease (disorder)
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system (disorder)\Disorder of kidney and/or ureter (disorder)\Kidney disease\Cyst of kidney (disorder)\Congenital cystic kidney disease\Autosomal dominant polycystic kidney disease (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jul 2024. Module: IPS terminology module (core metadata concept)

Descriptions:

Id Description Lang Type Status Case? Module

3657944013 Autosomal dominant polycystic kidney disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) IPS terminology module (core metadata concept)

3657945014 Autosomal dominant polycystic kidney disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) IPS terminology module (core metadata concept)

3657946010 ADPKD - autosomal dominant polycystic kidney disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) IPS terminology module (core metadata concept)

3657947018 Inherited disease with characteristics of the development of cysts in the kidneys. The disease rarely causes any noticeable problems until the cysts grow large enough to affect renal function, usually between 30 and 60 years of age. Less commonly, children or older people may have noticeable symptoms. Two different genes are known to cause this disease PKD1 and PKD2. en Definition Active Entire term case sensitive (core metadata concept) IPS terminology module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Autosomal dominant polycystic kidney disease (disorder)	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
Autosomal dominant polycystic kidney disease (disorder)	Is a	Congenital cystic kidney disease	true	Inferred relationship	Some
Autosomal dominant polycystic kidney disease (disorder)	Associated morphology	Polycystic change	true	Inferred relationship	Some	1
Autosomal dominant polycystic kidney disease (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	1
Autosomal dominant polycystic kidney disease (disorder)	Finding site	Kidney structure	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

International Patient Summary

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3657944013	Autosomal dominant polycystic kidney disease (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	IPS terminology module (core metadata concept)
3657945014	Autosomal dominant polycystic kidney disease	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	IPS terminology module (core metadata concept)
3657946010	ADPKD - autosomal dominant polycystic kidney disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	IPS terminology module (core metadata concept)
3657947018	Inherited disease with characteristics of the development of cysts in the kidneys. The disease rarely causes any noticeable problems until the cysts grow large enough to affect renal function, usually between 30 and 60 years of age. Less commonly, children or older people may have noticeable symptoms. Two different genes are known to cause this disease PKD1 and PKD2.	en	Definition	Active	Entire term case sensitive (core metadata concept)	IPS terminology module (core metadata concept)