34187009: Severe myopia (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Eye / vision finding\Visual system disorder (disorder)\Disorder of vision\Disorder of refraction AND/OR accommodation (disorder)\Disorder of refraction\Myopia\Severe myopia

\Disease\Disorder of body system\Visual system disorder (disorder)\Disorder of vision\Disorder of refraction AND/OR accommodation (disorder)\Disorder of refraction\Myopia\Severe myopia

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2006. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

57091015 Severe myopia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

57092010 High myopia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

765679017 Severe myopia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

4501161000241115 myopie sévère fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

641691000274111 Hohe Myopie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

641701000274111 Schwere Myopie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Severe myopia	Is a	Myopia	true	Inferred relationship	Some
Severe myopia	Finding site	Eye structure	false	Inferred relationship	Some
Severe myopia	Finding site	The eye, ocular adnexa, afferent visual pathways, efferent visual pathways, and pupil innervation pathways	true	Inferred relationship	Some	1
Severe myopia	Severity	Severe	false	Inferred relationship	Some
Severe myopia	Interprets	Vision observable (observable entity)	false	Inferred relationship	Some	1
Severe myopia	Has interpretation	Abnormal	false	Inferred relationship	Some	1
Severe myopia	Interprets	Visual function	false	Inferred relationship	Some	1
Severe myopia	Has interpretation	Abnormal	false	Inferred relationship	Some	1
Severe myopia	Interprets	Visual function	false	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Forster-Fuchs' spot (disorder)	Is a	True	Severe myopia	Inferred relationship	Some
Degenerative progressive high myopia	Is a	True	Severe myopia	Inferred relationship	Some
A rare disorder characterized by the association of aplasia cutis congenita with high myopia, congenital nystagmus and cone-rod dysfunction. It has been described in two siblings (brother and sister). Transmission is autosomal dominant.	Is a	True	Severe myopia	Inferred relationship	Some
High myopia-sensorineural deafness syndrome is a rare genetic disease characterized by high myopia, typically ranging from -6.0 to -11.0 diopters, and moderate to profound, bilateral, progressive sensorineural hearing loss with prelingual-onset. Affected individuals do not present other systemic, ocular or connective tissue manifestations.	Is a	True	Severe myopia	Inferred relationship	Some
A rare, genetic, lens position anomaly disease characterized by bilateral congenital blepharoptosis, ectopia lentis and high grade myopia. Additional reported manifestations include abnormally long eye globes and signs of levator aponeurosis disinsertion. There have been no further descriptions in the literature since 1982.	Is a	True	Severe myopia	Inferred relationship	Some
A rare multiple congenital anomalies/dysmorphic syndrome characterized by severe intellectual deficit, Dandy-Walker malformation, macrocephaly, severe myopia, brachytelephalangy with short and broad fingernails, and dysmorphic facial features (such as thick eyebrows, synophrys, epicanthal folds, low-set ears, short philtrum, and high-arched palate). Additional reported manifestations include seizures and skeletal and genital anomalies, among others. There have been no further descriptions in the literature since 1989.	Is a	True	Severe myopia	Inferred relationship	Some
Rare, isolated myopia is a rare, genetic, refraction anomaly disorder characterized by non-syndromic severe myopia, which may be associated with cataract and vitreoretinal degeneration (retinal detachment) that may lead to blindness.	Is a	True	Severe myopia	Inferred relationship	Some
A rare developmental defect with connective tissue involvement characterized by joint hyperextensibility and multiple dislocations of large joints, severe myopia, and short stature. Other common features include retinal detachment, iris and chorioretinal coloboma, kyphoscoliosis and other spine deformities, pectus carinatum, talipes equinovarus, and progressive hearing loss.	Is a	True	Severe myopia	Inferred relationship	Some
A rare primary bone dysplasia characterized by micromelia with rhizomelic shortening, metaphyseal widening of the long bones, brachydactyly, small scapulae, micrognathia and thoracic insufficiency requiring tracheostomy and ventilation, and severe myopia and sensorineural hearing loss. Further dysmorphic craniofacial features include frontal bossing, proptosis, epicanthal folds, short nose, flat nasal bridge, anteverted nares, midfacial retrusion, and cleft palate.	Is a	True	Severe myopia	Inferred relationship	Some
Acquired progressive esotropia due to high myopia (disorder)	Due to	True	Severe myopia	Inferred relationship	Some	3

This concept is not in any reference sets