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723503006: Retinal degeneration, nanophthalmos, glaucoma syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3424860014 Retinal degeneration, nanophthalmos, glaucoma syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3424861013 Retinal degeneration, nanophthalmos, glaucoma syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3424862018 Mackay Shek Carr syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Retinal degeneration, nanophthalmos, glaucoma syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Retinal degeneration, nanophthalmos, glaucoma syndrome Is a Degeneration of retina true Inferred relationship Existential restriction modifier
Retinal degeneration, nanophthalmos, glaucoma syndrome Is a Congenital glaucoma true Inferred relationship Existential restriction modifier
Retinal degeneration, nanophthalmos, glaucoma syndrome Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Retinal degeneration, nanophthalmos, glaucoma syndrome Is a Nanophthalmia true Inferred relationship Existential restriction modifier
Retinal degeneration, nanophthalmos, glaucoma syndrome Associated morphology Congenital smallness true Inferred relationship Existential restriction modifier 2
Retinal degeneration, nanophthalmos, glaucoma syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Retinal degeneration, nanophthalmos, glaucoma syndrome Finding site Entire eye true Inferred relationship Existential restriction modifier 2
Retinal degeneration, nanophthalmos, glaucoma syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Retinal degeneration, nanophthalmos, glaucoma syndrome Associated morphology Pigmentary degeneration false Inferred relationship Existential restriction modifier 2
Retinal degeneration, nanophthalmos, glaucoma syndrome Finding site Retinal structure false Inferred relationship Existential restriction modifier 2
Retinal degeneration, nanophthalmos, glaucoma syndrome Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier 3
Retinal degeneration, nanophthalmos, glaucoma syndrome Finding site Entire eye false Inferred relationship Existential restriction modifier 3
Retinal degeneration, nanophthalmos, glaucoma syndrome Associated morphology Pigmentary degeneration true Inferred relationship Existential restriction modifier 1
Retinal degeneration, nanophthalmos, glaucoma syndrome Finding site Retinal structure true Inferred relationship Existential restriction modifier 1
Retinal degeneration, nanophthalmos, glaucoma syndrome Is a Congenital anomaly of retina true Inferred relationship Existential restriction modifier
Retinal degeneration, nanophthalmos, glaucoma syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Retinal degeneration, nanophthalmos, glaucoma syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Retinal degeneration, nanophthalmos, glaucoma syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Retinal degeneration, nanophthalmos, glaucoma syndrome Is a Developmental hereditary disorder 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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