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367647000: Fibrocystic change (morphologic abnormality)

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

Descriptions:

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
504876010 Fibrocystic change en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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 Only initial character 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

4 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Fibrocystic change Is a Dysplasia false Inferred relationship Existential restriction modifier (core metadata concept)
Fibrocystic change Is a Cyst (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept)
Fibrocystic change Is a Fibrosis (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Fibrocystic change, proliferative type with atypia Is a True Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept)
Fibrocystic change, proliferative type Is a True Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept)
Nonproliferative fibrocystic change Is a True Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept)
Nonproliferative fibrocystic disease (morphologic abnormality) Is a True Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept)
Congenital cystic liver disease NOS Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Medullary cystic disease (disorder) Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Nephronophthisis Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Medullary cystic disease, otherwise specified Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 2
Medullary cystic disease NOS Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 2
Other specified congenital cystic kidney disease Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 2
Other congenital cystic kidney disease NOS Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital cystic kidney disease NOS Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 2
[X]Other cystic kidney diseases Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 2
Medullary sponge kidney Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 2
Adult type polycystic kidney disease type 1 (disorder) Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 2
Adult type polycystic kidney disease type 2 (disorder) Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant polycystic kidney disease in childhood Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 2
Nephronophthisis - medullary cystic disease Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 2
Medullary sponge kidney with nephrocalcinosis Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 2
Medullary sponge kidney without nephrocalcinosis (disorder) Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 2
Fibrocystic kidney disease (disorder) Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 2
Medullary cystic disease, adult type Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
[EDTA] Polycystic kidneys, infantile (recessive) associated with renal failure Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 2
[EDTA] Polycystic kidneys, adult type (dominant) associated with renal failure Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 2
[EDTA] Medullary cystic disease, including nephronophthisis, associated with renal failure Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
polykystose rénale autosomique dominante Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 2
Polycystic kidney disease, infantile type Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 2
Microcystic renal disease Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital cystic disease of liver Associated morphology True Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Simple renal cyst Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital cystic kidney disease Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Solitary multilocular renal cyst Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 2
Medullary cystic kidney disease type 1 Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Infantile nephronophthisis (disorder) Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Adolescent nephronophthisis (disorder) Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Juvenile nephronophthisis (disorder) Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Fibrocystic disease of breast Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Medullary cystic kidney disease type 2 Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Adolescent nephronophthisis (disorder) Associated morphology True Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Medullary cystic kidney disease type 2 Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Nephronophthisis Associated morphology True Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Juvenile nephronophthisis (disorder) Associated morphology True Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Infantile nephronophthisis (disorder) Associated morphology True Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Medullary cystic disease (disorder) Associated morphology True Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Fibrocystic disease of breast Associated morphology True Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Medullary cystic kidney disease type 1 Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Medullary cystic disease, adult type Associated morphology True Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Nephronophthisis type 6 (disorder) Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Nephronophthisis type 4 (disorder) Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Nephronophthisis type 5 (disorder) Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Nephronophthisis type 5 (disorder) Associated morphology True Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Nephronophthisis type 4 (disorder) Associated morphology True Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Nephronophthisis type 6 (disorder) Associated morphology True Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Boichis syndrome Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 4
Joubert syndrome with oculorenal defect (disorder) Associated morphology False Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 3
UMOD-related autosomal dominant tubulointerstitial kidney disease Associated morphology True Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Mucin 1 related autosomal dominant tubulointerstitial kidney disease (disorder) Associated morphology True Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant tubulointerstitial kidney disease (disorder) Associated morphology True Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Adult familial nephronophthisis with spastic quadriparesia syndrome Associated morphology True Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 3
Joubert syndrome with oculorenal defect (disorder) Associated morphology True Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Nephronophthisis - medullary cystic disease Associated morphology True Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome (disorder) Associated morphology True Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 5
Fibrocystic kidney disease (disorder) Associated morphology True Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Renal dysplasia and retinal aplasia Associated morphology True Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Boichis syndrome Associated morphology True Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 2
Fibrocystic renal degeneration Associated morphology True Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 2
Fibrocystic change of left breast (finding) Associated morphology True Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1
Fibrocystic change of right breast (finding) Associated morphology True Fibrocystic change Inferred relationship Existential restriction modifier (core metadata concept) 1

This concept is not in any reference sets

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