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1003408005: Congenital dystrophy of cornea (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4168182019 Congenital dystrophy of cornea (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4168183012 Congenital corneal dystrophy en Synonym Active Entire term case insensitive SNOMED CT core module
4168184018 Congenital dystrophy of cornea en Synonym Active Entire term case insensitive SNOMED CT core module


7 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital dystrophy of cornea Is a Congenital anomaly of cornea true Inferred relationship Existential restriction modifier
Congenital dystrophy of cornea Is a Corneal dystrophy true Inferred relationship Existential restriction modifier
Congenital dystrophy of cornea Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital dystrophy of cornea Finding site Corneal structure true Inferred relationship Existential restriction modifier 1
Congenital dystrophy of cornea Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital dystrophy of cornea Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Francois syndrome Is a True Congenital dystrophy of cornea Inferred relationship Existential restriction modifier
Stern Lubinsky Durrie syndrome Is a True Congenital dystrophy of cornea Inferred relationship Existential restriction modifier
Ophthalmomandibulomelic dysplasia Is a True Congenital dystrophy of cornea Inferred relationship Existential restriction modifier
Congenital macular corneal dystrophy Is a True Congenital dystrophy of cornea Inferred relationship Existential restriction modifier
Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome Is a True Congenital dystrophy of cornea Inferred relationship Existential restriction modifier
Congenital hereditary endothelial dystrophy and perceptive deafness syndrome Is a True Congenital dystrophy of cornea Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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