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778021002: Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3737210015 Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3737212011 Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3747112019 Nanophthalmos, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome Finding site Retinal structure true Inferred relationship Existential restriction modifier 4
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome Associated morphology Hyaline body true Inferred relationship Existential restriction modifier 1
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome Is a Disorder of macula of retina true Inferred relationship Existential restriction modifier
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 4
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome Is a Microphthalmos true Inferred relationship Existential restriction modifier
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome Is a Hereditary disorder of nervous system false Inferred relationship Existential restriction modifier
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome Finding site Entire eye true Inferred relationship Existential restriction modifier 2
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome Associated morphology Congenital smallness true Inferred relationship Existential restriction modifier 2
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome Associated morphology Separation true Inferred relationship Existential restriction modifier 3
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome Finding site Structure of fovea centralis true Inferred relationship Existential restriction modifier 3
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome Is a Retinal detachment false Inferred relationship Existential restriction modifier
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome Is a Drusen of optic disc true Inferred relationship Existential restriction modifier
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome Is a Autosomal recessive retinitis pigmentosa true Inferred relationship Existential restriction modifier
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome Finding site Optic disc structure true Inferred relationship Existential restriction modifier 1
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome Is a Inherited optic neuropathy true Inferred relationship Existential restriction modifier
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome Is a Hereditary degenerative disease of central nervous system true Inferred relationship Existential restriction modifier
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome Is a Optic disc disorder true Inferred relationship Existential restriction modifier
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome Is a Congenital retinoschisis false Inferred relationship Existential restriction modifier
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome Is a Retinoschisis true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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