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125291005: Multiple cysts (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
193781014 Multiple cysts en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
729099019 Multiple cysts (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Multiple cysts Is a Cyst true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Multicystic encephalomalacia Associated morphology False Multiple cysts Inferred relationship Some 1
Endoscopic de-roofing of multiple cysts of kidney (procedure) Direct morphology False Multiple cysts Inferred relationship Some 1
Multicystic encephalomalacia Associated morphology True Multiple cysts Inferred relationship Some 1
Endoscopic de-roofing of multiple cysts of kidney (procedure) Direct morphology False Multiple cysts Inferred relationship Some 1
A rare, nonprogressive, neurological disorder marked by intellectual deficit, spasticity and motor retardation associated with characteristic MRI findings of anterior bilateral temporal lobe cysts and multilobar leukoencephalopathy. So far, around 30 cases have been reported in the literature. Onset occurs in the first few months of life. Sensorineural deafness and microcephaly have also been reported. The etiology is unknown but an autosomal recessive mode of inheritance has been suggested. Associated morphology True Multiple cysts Inferred relationship Some 2
Endoscopic de-roofing of multiple cysts of kidney (procedure) Direct morphology True Multiple cysts Inferred relationship Some 2
Acquired neonatal pulmonary cysts Associated morphology True Multiple cysts Inferred relationship Some 1
Multiple renal cysts Associated morphology True Multiple cysts Inferred relationship Some 1
Multiple acquired kidney cysts (disorder) Associated morphology True Multiple cysts Inferred relationship Some 1
Bilateral multicystic renal dysplasia (disorder) Associated morphology True Multiple cysts Inferred relationship Some 1
Bilateral multicystic renal dysplasia (disorder) Associated morphology True Multiple cysts Inferred relationship Some 3
A rare congenital anomaly of the kidney and urinary tract (CAKUT) in which one or both kidneys (unilateral or bilateral MCDK respectively) are large, distended by multiple cysts, and non-functional. Unilateral MCDK is typically asymptomatic if the other kidney is fully functional but may occasionally present with abdominal obstructive signs when the cysts become too large. Bilateral MCDK is considered a lethal entity and neonates present with features of the Potter sequence, severe pulmonary hypoplasia and severe renal failure, and generally die shortly after birth. Associated morphology True Multiple cysts Inferred relationship Some 1
Multiple lung cysts Associated morphology True Multiple cysts Inferred relationship Some 2
Multiple cysts of breast Associated morphology True Multiple cysts Inferred relationship Some 1
Benign sebum filled cysts. Is a True Multiple cysts Inferred relationship Some
A rare congenital anomaly in which one kidney is large, distended by multiple cysts and non-functional. Unilateral multicystic kidney disease is typically asymptomatic if the other kidney is fully functional but may occasionally present with abdominal obstructive signs when the cysts become too large. Associated morphology True Multiple cysts Inferred relationship Some 1
Multiple embryonic cysts Is a True Multiple cysts Inferred relationship Some
Schöpf-Schulz-Passarge syndrome Associated morphology True Multiple cysts Inferred relationship Some 5

This concept is not in any reference sets

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