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367647000: Fibrocystic change (morphologic abnormality)

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1490803012 Fibrocystic changes en Synonym Active Case insensitive SNOMED CT core
504876010 Fibrocystic change en Synonym Active Case insensitive SNOMED CT core
823414011 Fibrocystic change (morphologic abnormality) en Fully specified name Active Case insensitive SNOMED CT core

4 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Fibrocystic change Is a Cyst true Inferred relationship Some
Fibrocystic change Is a Fibrosis true Inferred relationship Some
Fibrocystic change Is a Dysplasia false Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Joubert syndrome with oculorenal defect Associated morphology True Fibrocystic change Inferred relationship Some 1
Nephronophthisis - medullary cystic disease Associated morphology True Fibrocystic change Inferred relationship Some 1
RHYNS syndrome 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
Boichis syndrome 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 Associated morphology True Fibrocystic change Inferred relationship Some 1
Fibrocystic change of right breast Associated morphology True Fibrocystic change Inferred relationship Some 1
Nonproliferative fibrocystic disease Is a True Fibrocystic change Inferred relationship Some
Congenital cystic liver disease NOS Associated morphology False Fibrocystic change Inferred relationship Some 1
Medullary cystic kidney disease Associated morphology False Fibrocystic change Inferred relationship Some 1
Nephronophthisis Associated morphology False Fibrocystic change Inferred relationship Some 1
Medullary cystic disease OS 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 Associated morphology False Fibrocystic change Inferred relationship Some 2
Adult type polycystic kidney disease type 2 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 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
Polycystic kidney disease, adult type 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
Polycystic kidney disease Associated morphology False Fibrocystic change Inferred relationship Some 1
Solitary multilocular renal cyst Associated morphology False Fibrocystic change Inferred relationship Some 2
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
Medullary cystic kidney disease type 1 Associated morphology False Fibrocystic change Inferred relationship Some 1
Infantile nephronophthisis Associated morphology False Fibrocystic change Inferred relationship Some 1
Adolescent nephronophthisis Associated morphology False Fibrocystic change Inferred relationship Some 1
Juvenile nephronophthisis Associated morphology False Fibrocystic change Inferred relationship Some 1
Fibrocystic disease of breast Associated morphology False Fibrocystic change Inferred relationship Some 1
Medullary cystic kidney disease type 2 Associated morphology False Fibrocystic change Inferred relationship Some 1
Adolescent nephronophthisis Associated morphology True Fibrocystic change Inferred relationship Some 1
Medullary cystic kidney disease type 2 Associated morphology False Fibrocystic change Inferred relationship Some 1
Nephronophthisis Associated morphology True Fibrocystic change Inferred relationship Some 1
Juvenile nephronophthisis Associated morphology True Fibrocystic change Inferred relationship Some 1
Infantile nephronophthisis Associated morphology True Fibrocystic change Inferred relationship Some 1
Medullary cystic kidney disease Associated morphology True Fibrocystic change Inferred relationship Some 1
Fibrocystic disease of breast Associated morphology True Fibrocystic change Inferred relationship Some 1
Medullary cystic kidney disease 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 Associated morphology False Fibrocystic change Inferred relationship Some 1
Nephronophthisis type 4 Associated morphology False Fibrocystic change Inferred relationship Some 1
Nephronophthisis type 5 Associated morphology False Fibrocystic change Inferred relationship Some 1
Nephronophthisis type 5 Associated morphology True Fibrocystic change Inferred relationship Some 1
Nephronophthisis type 4 Associated morphology True Fibrocystic change Inferred relationship Some 1
Nephronophthisis type 6 Associated morphology True Fibrocystic change Inferred relationship Some 1
Boichis syndrome Associated morphology False Fibrocystic change Inferred relationship Some 4
Joubert syndrome with oculorenal defect Associated morphology False Fibrocystic change Inferred relationship Some 3
Autosomal dominant medullary cystic kidney disease with hyperuricaemia Associated morphology True Fibrocystic change Inferred relationship Some 1
MUC1-related autosomal dominant tubulointerstitial kidney disease 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 Associated morphology True Fibrocystic change Inferred relationship Some 3

Reference Sets

Body structure foundation reference set

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