367647000: fibrocysteuze verandering (afwijkende morfologie)

SNOMED CT Concept\Body structure\Morphologically altered structure\Morphologically abnormal structure (morphologic abnormality)\...

\Mechanical abnormality\Mechanical lesion\Cyst\Fibrocystic change

\Lesion (morphologic abnormality)\Mechanical lesion\Cyst\Fibrocystic change
\Lesion (morphologic abnormality)\Fibrosis AND/OR repair abnormality\Fibrosis\Fibrocystic change
\Lesion (morphologic abnormality)\Mass\Cyst\Fibrocystic change

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
Fibrocystic change	Is a	Dysplasia	false	Inferred relationship	Some
Fibrocystic change	Is a	Cyst	true	Inferred relationship	Some
Fibrocystic change	Is a	Fibrosis	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Fibrocystic change, proliferative type with atypia	Is a	True	Fibrocystic change	Inferred relationship	Some
Fibrocystic change, proliferative type	Is a	True	Fibrocystic change	Inferred relationship	Some
Nonproliferative fibrocystic change	Is a	True	Fibrocystic change	Inferred relationship	Some
Nonproliferative fibrocystic disease (morphologic abnormality)	Is a	True	Fibrocystic change	Inferred relationship	Some
Congenital cystic liver disease NOS	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	1
Medullary cystic disease of the kidney	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	1
Nephronophthisis	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	1
Medullary cystic disease, otherwise specified	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	2
Medullary cystic disease NOS	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	2
Other specified congenital cystic kidney disease	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	2
Other congenital cystic kidney disease NOS	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	2
Congenital cystic kidney disease NOS	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	2
[X]Other cystic kidney diseases	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	2
Medullary sponge kidney	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	2
Adult type polycystic kidney disease type 1 (disorder)	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	2
Adult type polycystic kidney disease type 2 (disorder)	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	2
Autosomal dominant polycystic kidney disease in childhood	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	2
Nephronophthisis - medullary cystic disease (disorder)	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	2
Medullary sponge kidney with nephrocalcinosis	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	2
Medullary sponge kidney without nephrocalcinosis	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	2
Fibrocystic kidney disease	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	2
Medullary cystic disease, adult type	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	1
[EDTA] Polycystic kidneys, infantile (recessive) associated with renal failure	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	2
[EDTA] Polycystic kidneys, adult type (dominant) associated with renal failure	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	2
[EDTA] Medullary cystic disease, including nephronophthisis, associated with renal failure	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	1
autosomaal dominante polycysteuze nierziekte	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	2
Polycystic kidney disease, infantile type	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	2
Microcystic renal disease	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	2
Congenital cystic disease of liver	Associated morphology	True	Fibrocystic change	Inferred relationship	Some	1
Simple renal cyst	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	3
Congenital cystic kidney disease	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	1
Solitary multilocular renal cyst	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	2
medullair-cystische nier type 1	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	1
Infantile nephronophthisis (disorder)	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	1
Adolescent nephronophthisis (disorder)	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	1
Juvenile nephronophthisis (disorder)	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	1
Fibrocystic disease of breast	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	1
medullair-cystische nier type 2	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	1
Adolescent nephronophthisis (disorder)	Associated morphology	True	Fibrocystic change	Inferred relationship	Some	1
medullair-cystische nier type 2	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	1
Nephronophthisis	Associated morphology	True	Fibrocystic change	Inferred relationship	Some	1
Juvenile nephronophthisis (disorder)	Associated morphology	True	Fibrocystic change	Inferred relationship	Some	1
Infantile nephronophthisis (disorder)	Associated morphology	True	Fibrocystic change	Inferred relationship	Some	1
Medullary cystic disease of the kidney	Associated morphology	True	Fibrocystic change	Inferred relationship	Some	1
Fibrocystic disease of breast	Associated morphology	True	Fibrocystic change	Inferred relationship	Some	1
medullair-cystische nier type 1	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	1
Medullary cystic disease, adult type	Associated morphology	True	Fibrocystic change	Inferred relationship	Some	1
Nephronophthisis type 6 (disorder)	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	1
Nephronophthisis type 4 (disorder)	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	1
Nephronophthisis type 5 (disorder)	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	1
Nephronophthisis type 5 (disorder)	Associated morphology	True	Fibrocystic change	Inferred relationship	Some	1
Nephronophthisis type 4 (disorder)	Associated morphology	True	Fibrocystic change	Inferred relationship	Some	1
Nephronophthisis type 6 (disorder)	Associated morphology	True	Fibrocystic change	Inferred relationship	Some	1
Nephronophthisis hepatic fibrosis syndrome (disorder)	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	4
Joubert syndrome with oculorenal defect (disorder)	Associated morphology	False	Fibrocystic change	Inferred relationship	Some	3
UMOD-related autosomal dominant tubulointerstitial kidney disease	Associated morphology	True	Fibrocystic change	Inferred relationship	Some	1
Mucin 1 related autosomal dominant tubulointerstitial kidney disease (disorder)	Associated morphology	True	Fibrocystic change	Inferred relationship	Some	1
Autosomal dominant tubulointerstitial kidney disease	Associated morphology	True	Fibrocystic change	Inferred relationship	Some	1
Adult familial nephronophthisis with spastic quadriparesia syndrome (disorder)	Associated morphology	True	Fibrocystic change	Inferred relationship	Some	3
Joubert syndrome with oculorenal defect (disorder)	Associated morphology	True	Fibrocystic change	Inferred relationship	Some	1
Nephronophthisis - medullary cystic disease (disorder)	Associated morphology	True	Fibrocystic change	Inferred relationship	Some	1
Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome (disorder)	Associated morphology	True	Fibrocystic change	Inferred relationship	Some	5
Fibrocystic kidney disease	Associated morphology	True	Fibrocystic change	Inferred relationship	Some	1
Renal dysplasia and retinal aplasia	Associated morphology	True	Fibrocystic change	Inferred relationship	Some	1
Nephronophthisis hepatic fibrosis syndrome (disorder)	Associated morphology	True	Fibrocystic change	Inferred relationship	Some	2
Fibrocystic renal degeneration	Associated morphology	True	Fibrocystic change	Inferred relationship	Some	2
Fibrocystic change of left breast (finding)	Associated morphology	True	Fibrocystic change	Inferred relationship	Some	1
Fibrocystic change of right breast (finding)	Associated morphology	True	Fibrocystic change	Inferred relationship	Some	1

Reference Sets

Dutch pathology simple reference set (foundation metadata concept)

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Id	Description	Lang	Type	Status	Case?	Module
504876010	Fibrocystic change	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
823414011	Fibrocystic change (morphologic abnormality)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1490803012	Fibrocystic changes	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1187701000146112	fibrocystische verandering	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
1187711000146114	fibrocysteuze verandering (afwijkende morfologie)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
1868801000146113	fibrocysteuze verandering	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)