FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.3  |  FHIR Version n/a  User: [n/a]

67046006: Structure of fovea centralis (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
111365015 Fovea centralis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
500593012 Structure of fovea centralis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
806727013 Structure of fovea centralis (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1232871016 Fovea centralis of retina en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1783832015 Centre of fovea en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1783833013 Centre of macula en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1784220016 Center of fovea en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1784221017 Center of macula en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3193421000005117 struktur af fovea centralis da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

3 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Structure of fovea centralis Is a Macula lutea structure true Inferred relationship Some
Structure of fovea centralis del af Entire macula lutea false Additional relationship Some
Structure of fovea centralis Laterality Side true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Entire fovea centralis Is a True Structure of fovea centralis Inferred relationship Some
Absent foveal reflex Finding site True Structure of fovea centralis Inferred relationship Some 1
Simultaneous perception Finding site False Structure of fovea centralis Inferred relationship Some
Superimposition Finding site True Structure of fovea centralis Inferred relationship Some 2
Foveola Is a True Structure of fovea centralis Inferred relationship Some
Subfoveal haemorrhage Finding site False Structure of fovea centralis Inferred relationship Some 1
Congenital hypoplasia of fovea centralis (disorder) Finding site False Structure of fovea centralis Inferred relationship Some 1
Subfoveal haemorrhage Finding site False Structure of fovea centralis Inferred relationship Some 1
Congenital hypoplasia of fovea centralis (disorder) Finding site True Structure of fovea centralis Inferred relationship Some 1
Congenital hypoplasia of fovea centralis (disorder) Finding site False Structure of fovea centralis Inferred relationship Some 2
A rare genetic non-syndromic developmental defect of the eye disorder with the association of posterior microphthalmia, retinal dystrophy compatible with retinitis pigmentosa, localised foveal schisis and optic disc drusen. Patients present high hyperopia, usually adult-onset progressive nyctalopia and reduced visual acuity and on occasion acute-angle glaucoma. Caused by homozygous or compound heterozygous mutation in the MFRP gene on chromosome 11q23. Finding site True Structure of fovea centralis Inferred relationship Some 3
A rare genetic ocular disease with characteristics of congenital nystagmus (horizontal, vertical and/or torsional), foveal hypoplasia, presenile cataracts (with typical onset in the second to third decade of life) and normal irides. Corneal pannus and/or optic nerve hypoplasia may also be present. Caused by heterozygous mutation in the PAX6 gene on chromosome 11p13. Finding site True Structure of fovea centralis Inferred relationship Some 1
A rare genetic eye disease with characteristics of foveal hypoplasia, optic nerve misrouting with an increased number of axons decussating at the optic chiasm and innervating the contralateral cortex, and posterior embryotoxon or Axenfeld anomaly (indicating anterior segment dysgenesis), in the absence of albinism. Patients present congenital nystagmus, decreased visual acuity, refractive errors and occasionally strabismus. Microphthalmia and retinochoroidal coloboma may also be associated. There is the disease is caused by homozygous or compound heterozygous mutation in the SLC38A8 gene on chromosome 16q23. Finding site True Structure of fovea centralis Inferred relationship Some 3
Impending macular hole Finding site True Structure of fovea centralis Inferred relationship Some 1
A rare macular disorder characterized mostly by a variable degree of decreased visual acuity, jerk or pendular nystagmus, and typical ocular findings at imaging. The disease is usually bilateral. Rarely, nystagmus can be absent. Locally, the disease is characterized by underdeveloped foveal pit, absence of foveal pigmentation and/or foveal avascular zone, and persistence of inner retinal layers at the fovea, in absence of concomitant ocular or systemic pathology. Finding site True Structure of fovea centralis Inferred relationship Some 1
Myopic foveoschisis Finding site True Structure of fovea centralis Inferred relationship Some 1
Myopic foveoschisis Finding site True Structure of fovea centralis Inferred relationship Some 2

Reference Sets

Lateralizable body structure reference set (foundation metadata concept)

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

Back to Start