FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

28726007: Corneal structure (body structure)

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
48095018 Cornea en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
483964014 Corneal structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
759438018 Corneal structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
891011000172119 structure cornéenne fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
969991000172119 cornée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
971911000172116 structure de la cornée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

76 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Corneal structure Is a Conjunctival and/or corneal structures (body structure) true Inferred relationship Some
Corneal structure Is a Outer coating of eyeball; has parts cornea and sclera true Inferred relationship Some
Corneal structure partie de Entire anterior segment of eyeball false Additional relationship Some
Corneal structure partie de Entire tunica fibrosa of eyeball false Additional relationship Some
Corneal structure Laterality Side (qualifier value) true Inferred relationship Some
Corneal structure Is a Anterior eyeball segment structure false Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Penetrating keratoplasty Procedure site - Direct (attribute) True Corneal structure Inferred relationship Some 2
Penetrating keratoplasty with homograft Procedure site - Direct (attribute) True Corneal structure Inferred relationship Some 1
Repair of postcataract wound dehiscence with conjunctival flap Procedure site - Direct (attribute) True Corneal structure Inferred relationship Some 2
Conjunctival flap, total Procedure site - Direct (attribute) True Corneal structure Inferred relationship Some 2
Conjunctival flap, partial Procedure site - Direct (attribute) True Corneal structure Inferred relationship Some 2
Recurrent infection of cornea caused by human herpes simplex virus (disorder) Finding site True Corneal structure Inferred relationship Some 1
Recurrent inflammation of cornea caused by human herpes simplex virus (disorder) Finding site True Corneal structure Inferred relationship Some 1
Congenital corneal leucoma Finding site True Corneal structure Inferred relationship Some 1
Neurotrophic keratitis due to diabetes mellitus (disorder) Finding site True Corneal structure Inferred relationship Some 2
Corneal deposits due to metabolic disorder Finding site True Corneal structure Inferred relationship Some 1
Contact lens-associated corneal infiltrates due to hypoxia Finding site True Corneal structure Inferred relationship Some 1
Penetrating keratoplasty with implantation of posterior chamber intraocular lens (procedure) Procedure site - Direct (attribute) True Corneal structure Inferred relationship Some 1
Penetrating keratoplasty with implantation of posterior chamber intraocular lens (procedure) Procedure site - Direct (attribute) True Corneal structure Inferred relationship Some 3
Penetrating keratoplasty with implantation of posterior chamber intraocular lens (procedure) Procedure site - Direct (attribute) True Corneal structure Inferred relationship Some 4
Adjustable refractive surgery (procedure) Procedure site - Direct (attribute) False Corneal structure Inferred relationship Some 2
Corneal leukoma (disorder) Finding site True Corneal structure Inferred relationship Some 2
Congenital corneal leucoma Finding site True Corneal structure Inferred relationship Some 2
Iatrogenic corneal ectasia Finding site True Corneal structure Inferred relationship Some 1
Post-surgical neurotrophic keratitis Finding site True Corneal structure Inferred relationship Some 2
Neurotrophic keratitis following herpes simplex dendritic keratitis Finding site True Corneal structure Inferred relationship Some 2
Corneal ghost vessels Finding site True Corneal structure Inferred relationship Some 2
Post-surgical corneal haze Finding site False Corneal structure Inferred relationship Some 1
Opacity of cornea due to and following traumatic injury (disorder) Finding site True Corneal structure Inferred relationship Some 1
Keratitis caused by parasite (disorder) Finding site True Corneal structure Inferred relationship Some 1
Vitreous touch syndrome Finding site True Corneal structure Inferred relationship Some 1
Keratocentesis Procedure site - Direct (attribute) True Corneal structure Inferred relationship Some 1
LCAT (lecithin-cholesterol acyltransferase) deficiency is a rare lipoprotein metabolism disorder characterized clinically by corneal opacities, and sometimes renal failure and hemolytic anemia, and biochemically by severely reduced HDL cholesterol. Finding site True Corneal structure Inferred relationship Some 1
Fish eye disease (FED) is a form of genetic LCAT (lecithin-cholesterol acyltransferase) deficiency characterized clinically by corneal opacifications, and biochemically by significantly reduced HDL cholesterol and partial LCAT enzyme deficiency. Finding site True Corneal structure Inferred relationship Some 2
A form of lecithin-cholesterol acyltransferase deficiency (LCAT) characterized clinically by corneal opacities, hemolytic anemia and renal failure and biochemically by severely decreased HDL cholesterol and complete deficiency of the LCAT enzyme. Age of onset and severity of clinical manifestations are variable. Caused by mutations in the LCAT gene (16q22.1) encoding the LCAT enzyme which catalyzes the formation of cholesterol esters in lipoproteins, leading to progressive lipid deposition in body tissues. There is no clear genotype-phenotype correlation since family members with the same mutation have been found to have different clinical and biochemical pictures. Environmental factors or other minor genes may therefore also be involved in the disorder. Finding site True Corneal structure Inferred relationship Some 1
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by developmental delay with intellectual disability, postnatal growth deficiency causing profound limb shortening with proximal and distal segments involvement, narrow chest, abnormalities of the spine, pelvis, and metaphyses, corneal clouding, and patent ductus arteriosus. Dysmorphic facial features include hypertelorism, prominent eyes, depressed nasal bridge, and short upturned nose. Finding site True Corneal structure Inferred relationship Some 2
Dehiscence of corneal transplant wound (disorder) Finding site True Corneal structure Inferred relationship Some 1
Harvesting of cornea Procedure site - Direct (attribute) True Corneal structure Inferred relationship Some 1
A rare genetic eye disease characterized by congenital cataract, microcornea, and corneal opacity, resulting in severe visual impairment or blindness. Depending on the genetic background, other developmental ocular defects may also be present. Finding site True Corneal structure Inferred relationship Some 2
A rare genetic eye disease characterized by congenital cataract, microcornea, and corneal opacity, resulting in severe visual impairment or blindness. Depending on the genetic background, other developmental ocular defects may also be present. Finding site True Corneal structure Inferred relationship Some 3
Corneal staphyloma Finding site True Corneal structure Inferred relationship Some 2
Congenital anterior staphyloma Finding site True Corneal structure Inferred relationship Some 4
Keratoglobus (disorder) Finding site True Corneal structure Inferred relationship Some 1
Keratoglobus (disorder) Finding site False Corneal structure Inferred relationship Some 2
Infiltrate of cornea following laser assisted in situ keratomileusis (disorder) Finding site True Corneal structure Inferred relationship Some 1
Xerosis of cornea (finding) Finding site True Corneal structure Inferred relationship Some 1
A rare genetic neurometabolic disease with characteristics of prenatal and postnatal growth retardation, hypotonia, failure to thrive, large and late-closing fontanel, development delay, cutis laxa, joint laxity, progeroid appearance and dysmorphic facial features. In addition, corneal opacities, cataracts, myopia, seizures, hyperreflexia and athetoid movements have also been associated. Finding site True Corneal structure Inferred relationship Some 1
Pyrroline-5-carboxylate reductase 1 related de Barsy syndrome Finding site True Corneal structure Inferred relationship Some 1
Calculation of corneal tissue ablation depth for refractive change (procedure) Procedure site - Indirect (attribute) True Corneal structure Inferred relationship Some 1
Excision of pterygium with corneal transplant (procedure) Procedure site - Direct (attribute) True Corneal structure Inferred relationship Some 3
Toric photorefractive keratectomy (procedure) Procedure site - Indirect (attribute) True Corneal structure Inferred relationship Some 3
Lamellar keratoplasty with autograft Procedure site - Direct (attribute) True Corneal structure Inferred relationship Some 1
Repair of filtering bleb by corneal graft Procedure site - Direct (attribute) True Corneal structure Inferred relationship Some 2
A rare ophthalmic disorder characterized by periodic inflammatory attacks of the cornea manifesting as unilateral ocular pain, conjunctival hyperemia, photophobia and epiphora lasting for 1 to 3 days, followed by blurred vision for several weeks. Caused by a heterozygous pathogenic variant c.61G>C, p.(Asp21His) in the NLRP3 gene. The pathogenic variant is highly penetrant (95%). The disease is autosomal dominant. Finding site True Corneal structure Inferred relationship Some 2
Disorder of cornea following cataract surgery Finding site True Corneal structure Inferred relationship Some 2
Ab interno canaloplasty Procedure site - Direct (attribute) False Corneal structure Inferred relationship Some 1
Corneal thinning (finding) Finding site True Corneal structure Inferred relationship Some 2
Removal of foreign body of cornea by incision Procedure site - Direct (attribute) True Corneal structure Inferred relationship Some 2
Peripheral anterior synechiae in nasal quadrant of angle Finding site True Corneal structure Inferred relationship Some 3
Peripheral anterior synechiae in temporal quadrant of iridocorneal angle (disorder) Finding site True Corneal structure Inferred relationship Some 3
Peripheral anterior synechiae in inferior quadrant of angle Finding site True Corneal structure Inferred relationship Some 3
Peripheral anterior synechiae in superior quadrant of iridocorneal angle (disorder) Finding site True Corneal structure Inferred relationship Some 3
Ab interno canaloplasty Procedure site - Direct (attribute) True Corneal structure Inferred relationship Some 3
Serpiginous ulcer of cornea (disorder) Finding site True Corneal structure Inferred relationship Some 1
Mitomycin intravascular chemoembolization of cornea Procedure site - Direct (attribute) True Corneal structure Inferred relationship Some 1
Corneal disorder caused by monkeypox virus Finding site True Corneal structure Inferred relationship Some 1

Start Previous Page 25 of 25

Reference Sets

Lateralizable body structure reference set (foundation metadata concept)

Anatomy structure and entire association reference set (foundation metadata concept)

Anatomy structure and part association reference set (foundation metadata concept)

Back to Start