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717915004: Blepharoptosis, myopia, ectopia lentis syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3324394016 Blepharoptosis, myopia, ectopia lentis syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3324396019 Blepharoptosis, myopia, ectopia lentis 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
Blepharoptosis, myopia, ectopia lentis syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Blepharoptosis, myopia, ectopia lentis syndrome Is a Congenital ptosis true Inferred relationship Existential restriction modifier
Blepharoptosis, myopia, ectopia lentis syndrome Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Blepharoptosis, myopia, ectopia lentis syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Blepharoptosis, myopia, ectopia lentis syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Blepharoptosis, myopia, ectopia lentis syndrome Finding site Structure of lens of eye true Inferred relationship Existential restriction modifier 2
Blepharoptosis, myopia, ectopia lentis syndrome Associated morphology Congenital prolapse false Inferred relationship Existential restriction modifier 3
Blepharoptosis, myopia, ectopia lentis syndrome Finding site Upper eyelid structure false Inferred relationship Existential restriction modifier 3
Blepharoptosis, myopia, ectopia lentis syndrome Is a Severe myopia true Inferred relationship Existential restriction modifier
Blepharoptosis, myopia, ectopia lentis syndrome Is a Congenital ectopic lens true Inferred relationship Existential restriction modifier
Blepharoptosis, myopia, ectopia lentis syndrome Associated morphology Congenital ectopia true Inferred relationship Existential restriction modifier 2
Blepharoptosis, myopia, ectopia lentis syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Blepharoptosis, myopia, ectopia lentis syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Blepharoptosis, myopia, ectopia lentis syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Blepharoptosis, myopia, ectopia lentis syndrome Finding site Upper eyelid structure true Inferred relationship Existential restriction modifier 1
Blepharoptosis, myopia, ectopia lentis syndrome Associated morphology Prolapse true Inferred relationship Existential restriction modifier 1
Blepharoptosis, myopia, ectopia lentis 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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