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232065000: Goldmann-Favre syndrome (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
347717017 Goldmann-Favre syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
620082013 Goldmann-Favre syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
5072496019 Enhanced S-cone syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5072497011 Retinoschisis with early nyctalopia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5072498018 A vitreoretinal dystrophy with characteristics of early onset of night blindness, reduced bilateral visual acuity, and typical fundus findings (progressive pigmentary degenerative changes, macular edema, retinoschisis). The onset is usually in childhood. Mutations in the NR2E3 gene (formerly called PNR) have been identified in some patients. NR2E3 (15q23) encodes a retinal nuclear receptor that is involved in the differentiation of photoreceptors. Inherited as an autosomal recessive trait and has a progressive course. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5072499014 A vitreoretinal dystrophy with characteristics of early onset of night blindness, reduced bilateral visual acuity, and typical fundus findings (progressive pigmentary degenerative changes, macular oedema, retinoschisis). The onset is usually in childhood. Mutations in the NR2E3 gene (formerly called PNR) have been identified in some patients. NR2E3 (15q23) encodes a retinal nuclear receptor that is involved in the differentiation of photoreceptors. Inherited as an autosomal recessive trait and has a progressive course. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
347717017 Goldmann-Favre syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
620082013 Goldmann-Favre syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
620082013 Goldmann-Favre syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
5072496019 Enhanced S-cone syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5072497011 Retinoschisis with early nyctalopia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5072498018 A vitreoretinal dystrophy with characteristics of early onset of night blindness, reduced bilateral visual acuity, and typical fundus findings (progressive pigmentary degenerative changes, macular edema, retinoschisis). The onset is usually in childhood. Mutations in the NR2E3 gene (formerly called PNR) have been identified in some patients. NR2E3 (15q23) encodes a retinal nuclear receptor that is involved in the differentiation of photoreceptors. Inherited as an autosomal recessive trait and has a progressive course. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5072499014 A vitreoretinal dystrophy with characteristics of early onset of night blindness, reduced bilateral visual acuity, and typical fundus findings (progressive pigmentary degenerative changes, macular oedema, retinoschisis). The onset is usually in childhood. Mutations in the NR2E3 gene (formerly called PNR) have been identified in some patients. NR2E3 (15q23) encodes a retinal nuclear receptor that is involved in the differentiation of photoreceptors. Inherited as an autosomal recessive trait and has a progressive course. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
544031000274114 Enhanced-S-Cone Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3388121001000111 Goldmann-Favre-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
906021000172111 syndrome de Goldmann-Favre fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
913521000172114 syndrome d'augmentation des cônes bleus fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
906021000172111 syndrome de Goldmann-Favre fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
913521000172114 syndrome d'augmentation des cônes bleus fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
544031000274114 Enhanced-S-Cone Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3388121001000111 Goldmann-Favre-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Goldmann-Favre syndrome Is a Retinal disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Goldmann-Favre syndrome Is a Hereditary vitreoretinopathy false Inferred relationship Existential restriction modifier (core metadata concept)
Goldmann-Favre syndrome Finding site Vitreous body structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Goldmann-Favre syndrome Finding site Retinal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Goldmann-Favre syndrome Is a Chronic disease of ocular adnexa true Inferred relationship Existential restriction modifier (core metadata concept)
Goldmann-Favre syndrome Is a Connective tissue hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Goldmann-Favre syndrome Is a Vitreous degeneration (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Goldmann-Favre syndrome Is a Vitreoretinal dystrophy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Goldmann-Favre syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Goldmann-Favre syndrome Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 3
Goldmann-Favre syndrome Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 2
Goldmann-Favre syndrome Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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