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232053004: Autosomal recessive retinitis pigmentosa (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
347704015 Autosomal recessive retinitis pigmentosa en Synonym Active Entire term case insensitive SNOMED CT core module
620068013 Autosomal recessive retinitis pigmentosa (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


17 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal recessive retinitis pigmentosa Is a Retinitis pigmentosa true Inferred relationship Existential restriction modifier
Autosomal recessive retinitis pigmentosa Finding site Retinal structure false Inferred relationship Existential restriction modifier
Autosomal recessive retinitis pigmentosa Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Autosomal recessive retinitis pigmentosa Finding site Retinal structure true Inferred relationship Existential restriction modifier 1
Autosomal recessive retinitis pigmentosa Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
Oculotrichodysplasia Is a True Autosomal recessive retinitis pigmentosa Inferred relationship Existential restriction modifier
Spastic tetraplegia, retinitis pigmentosa, intellectual disability syndrome Is a True Autosomal recessive retinitis pigmentosa Inferred relationship Existential restriction modifier
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome Is a True Autosomal recessive retinitis pigmentosa Inferred relationship Existential restriction modifier
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome Is a True Autosomal recessive retinitis pigmentosa Inferred relationship Existential restriction modifier
Autosomal recessive posterior column ataxia and retinitis pigmentosa Is a True Autosomal recessive retinitis pigmentosa Inferred relationship Existential restriction modifier
Cleft lip retinopathy syndrome Is a True Autosomal recessive retinitis pigmentosa Inferred relationship Existential restriction modifier
Retinitis pigmentosa-deafness syndrome Is a True Autosomal recessive retinitis pigmentosa Inferred relationship Existential restriction modifier
Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome Is a True Autosomal recessive retinitis pigmentosa Inferred relationship Existential restriction modifier
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome Is a True Autosomal recessive retinitis pigmentosa Inferred relationship Existential restriction modifier
Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome Is a True Autosomal recessive retinitis pigmentosa Inferred relationship Existential restriction modifier
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome Is a True Autosomal recessive retinitis pigmentosa Inferred relationship Existential restriction modifier
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome Is a True Autosomal recessive retinitis pigmentosa Inferred relationship Existential restriction modifier
Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa Is a True Autosomal recessive retinitis pigmentosa Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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