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65194006: Night blindness (disorder)


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
108338011 Night blindness en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
108340018 Nyctalopia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
804670017 Night blindness (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1788108010 Difficulty seeing at night en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1042801000195118 cecità notturna it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
588321000172116 cécité nocturne fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
391371000274115 Nachtblindheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
646591000274119 Nyktalopie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


7 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Night blindness Is a Vision problem false Inferred relationship Some
Night blindness Is a Retinal disorder true Inferred relationship Some
Night blindness Finding site Retinal structure true Inferred relationship Some 1
Night blindness Is a Blindness AND/OR vision impairment level true Inferred relationship Some
Night blindness Interprets Vision observable (observable entity) false Inferred relationship Some 1
Night blindness Has interpretation Abnormal false Inferred relationship Some 2
Night blindness Has interpretation Impaired false Inferred relationship Some 1
Night blindness Interprets Vision, function (observable entity) false Inferred relationship Some 2
Night blindness Interprets Visual function false Inferred relationship Some 1
Night blindness Is a Retina finding (finding) false Inferred relationship Some
Night blindness Interprets Visual function false Inferred relationship Some 1
Night blindness Interprets Visual function false Inferred relationship Some 2
Night blindness Interprets Visual function false Inferred relationship Some 1
Night blindness Interprets Visual function false Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Abnormal dark adaptation curve Is a True Night blindness Inferred relationship Some
Acquired night blindness Is a True Night blindness Inferred relationship Some
Oguchi's disease Is a False Night blindness Inferred relationship Some
Unspecified night blindness Is a False Night blindness Inferred relationship Some
Hereditary night blindness NOS Is a False Night blindness Inferred relationship Some
Congenital night blindness NOS Is a False Night blindness Inferred relationship Some
Abnormal dark adaptive curve NOS Is a False Night blindness Inferred relationship Some
Night blindness NOS Is a False Night blindness Inferred relationship Some
Chondroectodermal dysplasia with night blindness is a rare genetic bone development disorder characterized by proportionate short stature, nail dysplasia (enlarged, convex, hypertrophic nails), hypodontia and night blindness. Osteopenia, a tendency to present fractures, talipes varus with abnormal gait, ear infections, and watering eyes due to narrow tear ducts are frequently associated. Radiologically patients present delayed bone age on wrist X-rays, platyspondyly, and broad metaphyses of humeri with dense and thickened growth plates. Is a True Night blindness Inferred relationship Some
Congenital stationary night blindness Is a True Night blindness Inferred relationship Some
A rare genetic multiple congenital anomalies/dysmorphic syndrome with characteristics of slowly progressive night blindness, skeletal abnormalities (sloping shoulders, joint hyperextensibility, minor radiological anomalies) and characteristic facial features (periorbital anomalies, malar flatness, retrognathia). Additional manifestations include myopia and extinguished electroretinograms. Is a True Night blindness Inferred relationship Some

This concept is not in any reference sets

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