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3679006: Polycystic 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
7209017 Polycystic change en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
768582017 Polycystic change (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Polycystic change Is a Cyst true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Other congenital cystic kidney disease NOS Associated morphology False Polycystic change Inferred relationship Some 2
Congenital cystic kidney disease NOS Associated morphology False Polycystic change Inferred relationship Some 2
Medullary cystic disease of the kidney Associated morphology False Polycystic change Inferred relationship Some 3
[EDTA] Polycystic kidneys, infantile (recessive) associated with renal failure Associated morphology False Polycystic change Inferred relationship Some 2
Medullary cystic disease, otherwise specified Associated morphology False Polycystic change Inferred relationship Some 2
Medullary cystic disease, adult type Associated morphology False Polycystic change Inferred relationship Some 3
Medullary sponge kidney without nephrocalcinosis Associated morphology False Polycystic change Inferred relationship Some 2
[EDTA] Medullary cystic disease, including nephronophthisis, associated with renal failure Associated morphology False Polycystic change Inferred relationship Some 3
Medullary sponge kidney with nephrocalcinosis Associated morphology False Polycystic change Inferred relationship Some 2
Fibrocystic kidney disease Associated morphology False Polycystic change Inferred relationship Some 2
Nephronophthisis - medullary cystic disease Associated morphology False Polycystic change Inferred relationship Some 3
Microcystic renal disease Associated morphology False Polycystic change Inferred relationship Some 2
Medullary sponge kidney Associated morphology False Polycystic change Inferred relationship Some 2
Nephronophthisis Associated morphology False Polycystic change Inferred relationship Some 3
Medullary cystic disease NOS Associated morphology False Polycystic change Inferred relationship Some 2
Other specified congenital cystic kidney disease Associated morphology False Polycystic change Inferred relationship Some 2
[X]Other cystic kidney diseases Associated morphology False Polycystic change Inferred relationship Some 2
Polycystic kidney disease, infantile type Associated morphology False Polycystic change Inferred relationship Some 2
Solitary multilocular renal cyst Associated morphology False Polycystic change Inferred relationship Some 2
Congenital cystic kidney disease Associated morphology False Polycystic change Inferred relationship Some 1
Simple renal cyst Associated morphology False Polycystic change Inferred relationship Some 2
Medullary cystic disease, otherwise specified Associated morphology False Polycystic change Inferred relationship Some 2
Microcystic renal disease Associated morphology False Polycystic change Inferred relationship Some 4
Congenital cystic kidney disease Associated morphology True Polycystic change Inferred relationship Some 2
Isolated polycystic liver disease (PCLD) is a genetic disorder characterized by the appearance of numerous cysts spread throughout the liver and that in most cases is described as autosomal dominant polycystic liver disease (ADPCLD). Associated morphology True Polycystic change Inferred relationship Some 1
Bilateral medullary sponge kidney (disorder) Associated morphology False Polycystic change Inferred relationship Some 3
Polycystic kidney disease, infantile type Associated morphology True Polycystic change Inferred relationship Some 1
Solitary multilocular renal cyst Associated morphology True Polycystic change Inferred relationship Some 1
Medullary sponge kidney Associated morphology True Polycystic change Inferred relationship Some 1
Medullary sponge kidney with nephrocalcinosis Associated morphology True Polycystic change Inferred relationship Some 1
Medullary sponge kidney without nephrocalcinosis Associated morphology True Polycystic change Inferred relationship Some 1
Fibrocystic kidney disease Associated morphology False Polycystic change Inferred relationship Some 1
Bilateral medullary sponge kidney (disorder) Associated morphology True Polycystic change Inferred relationship Some 1
Multinodular goiter - cystic kidney - polydactyly syndrome is a very rare syndrome characterized by the association of multinodular goiter, cystic renal disease and digital anomalies. Associated morphology False Polycystic change Inferred relationship Some 6
A rare genetic disease characterized by intrauterine growth retardation, permanent neonatal diabetes mellitus, and congenital hypothyroidism. Additional manifestations include congenital glaucoma, hepatic disease (hepatitis, fibrosis, and cirrhosis), polycystic kidneys, exocrine pancreatic dysfunction, sensorineural hearing impairment, developmental delay, and mild facial dysmorphism (such as flat nasal bridge, epicanthal folds, long philtrum, and low-set ears), among others. Associated morphology True Polycystic change Inferred relationship Some 1
Fibropolycystic disease of liver Associated morphology True Polycystic change Inferred relationship Some 3
Renal-hepatic-pancreatic dysplasia is a rare, genetic, developmental defect during embryogenesis syndrome characterized by the triad of pancreatic fibrosis (and cysts, with a reduction of parenchymal tissue), renal dysplasia (with peripheral cortical cysts, primitive collecting ducts, glomerular cysts and metaplastic cartilage) and hepatic dysgenesis (enlarged portal areas containing numerous elongated binary profiles with a tendency to perilobular fibrosis). Situs abnormalities, skeletal anomalies and anencephaly have also been associated. Patients that survive the neonatal period present renal insufficiency, chronic jaundice and insulin-dependent diabetes. Associated morphology True Polycystic change Inferred relationship Some 1
Adult type polycystic kidney disease type 2 (disorder) Associated morphology True Polycystic change Inferred relationship Some 1
Adult type polycystic kidney disease type 1 Associated morphology True Polycystic change Inferred relationship Some 1
Autosomal dominant polycystic kidney disease in childhood Associated morphology True Polycystic change Inferred relationship Some 1
A rare, genetic, renal tubular disease characterized by progressive outgrowths of fluid-filled cysts from the renal epithelium, which can manifest with hematuria, urinary tract infections, hypertension, and abdominal or flank pain. The slowly progressive loss of kidney function may evolve to end stage kidney disease (ESKD). Associated morphology True Polycystic change Inferred relationship Some 1
A rare contiguous gene syndrome involving a partial deletion of chromosome 16 and characterized by early-onset and severe polycystic kidney disease with various manifestations of tuberous sclerosis (multiple angiomyolipomas, lymphangioleiomyomatosis and periventricular calcifications of the central nervous system). Associated morphology True Polycystic change Inferred relationship Some 1
A rare contiguous gene syndrome involving a partial deletion of chromosome 16 and characterized by early-onset and severe polycystic kidney disease with various manifestations of tuberous sclerosis (multiple angiomyolipomas, lymphangioleiomyomatosis and periventricular calcifications of the central nervous system). Associated morphology False Polycystic change Inferred relationship Some 3
Polycystic spleen Associated morphology True Polycystic change Inferred relationship Some 1
Acquired polycystic kidney disease Associated morphology True Polycystic change Inferred relationship Some 1
Hepatic fibrosis-renal cysts-intellectual disability syndrome is a rare, syndromic intellectual disability characterized by early developmental delay with failure to thrive, intellectual disability, congenital hepatic fibrosis, renal cystic dysplasia, and dysmorphic facial features (bilateral ptosis, anteverted nostrils, high arched palate, and micrognathia). Variable additional features have been reported, including cerebellar anomalies, postaxial polydactyly, syndactyly, genital anomalies, tachypnea. There have been no further descriptions in the literature since 1987. Associated morphology True Polycystic change Inferred relationship Some 2
Multinodular goiter - cystic kidney - polydactyly syndrome is a very rare syndrome characterized by the association of multinodular goiter, cystic renal disease and digital anomalies. Associated morphology True Polycystic change Inferred relationship Some 3
NPHP3-related Meckel-like syndrome is a rare, genetic, syndromic renal malformation characterized by cystic renal dysplasia with or without prenatal oligohydramnios, central nervous system abnormalities (commonly Dandy-Walker malformation), congenital hepatic fibrosis, and absence of polydactyly. Associated morphology True Polycystic change Inferred relationship Some 2
Polycystic ovary syndrome Associated morphology True Polycystic change Inferred relationship Some 1
Polycystic ovary Associated morphology True Polycystic change Inferred relationship Some 1
Polycystic hydatid Associated morphology True Polycystic change Inferred relationship Some 1
Honeycomb appearance Is a True Polycystic change Inferred relationship Some
Microcystic renal disease Associated morphology True Polycystic change Inferred relationship Some 1
Bilateral medullary sponge kidney (disorder) Associated morphology True Polycystic change Inferred relationship Some 2
Polycystic left ovary Associated morphology True Polycystic change Inferred relationship Some 1
Polycystic right ovary (disorder) Associated morphology True Polycystic change Inferred relationship Some 1
Polycystic bilateral ovaries (disorder) Associated morphology True Polycystic change Inferred relationship Some 1
Polycystic bilateral ovaries (disorder) Associated morphology True Polycystic change Inferred relationship Some 2
Polycystic ovary syndrome of right ovary Associated morphology True Polycystic change Inferred relationship Some 1
Polycystic ovary syndrome of left ovary Associated morphology True Polycystic change Inferred relationship Some 1
Polycystic ovary syndrome of bilateral ovaries (disorder) Associated morphology True Polycystic change Inferred relationship Some 1
Polycystic ovary syndrome of bilateral ovaries (disorder) Associated morphology True Polycystic change Inferred relationship Some 2
polykystose hépatique autosomique dominante Associated morphology False Polycystic change Inferred relationship Some 1
Polycystic hydatid caused by Echinococcus oligarthra (disorder) Associated morphology True Polycystic change Inferred relationship Some 1
Polycystic hydatid caused by Echinococcus vogeli (disorder) Associated morphology True Polycystic change Inferred relationship Some 1
A rare genetic syndrome with a central nervous system malformation as a major feature, characterized by a triad of high alpha-fetoprotein levels in both maternal serum and amniotic fluid, cerebral ventriculomegaly, and renal macro- and microcysts. Variable findings include congenital nephrotic syndrome, aqueductal stenosis, gray matter heterotopias, and cardiac malformations, among others. Associated morphology True Polycystic change Inferred relationship Some 1
Polycystic liver disease-3 due to heterozygous mutation of ALG8 gene Associated morphology True Polycystic change Inferred relationship Some 1

This concept is not in any reference sets

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