FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.24  |  FHIR Version n/a  User: [n/a]

734026006: Isolated congenital megalocornea (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
3481980019 Isolated congenital megalocornea (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3481981015 Isolated congenital megalocornea en Synonym Active Entire term case insensitive SNOMED CT core module
3481982010 Congenital anterior megalophthalmia 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
Isolated congenital megalocornea Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier
Isolated congenital megalocornea Is a Megalocornea true Inferred relationship Existential restriction modifier
Isolated congenital megalocornea Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Isolated congenital megalocornea Associated morphology Congenital enlargement false Inferred relationship Existential restriction modifier 1
Isolated congenital megalocornea Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Isolated congenital megalocornea Finding site Corneal structure true Inferred relationship Existential restriction modifier 1
Isolated congenital megalocornea Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Isolated congenital megalocornea Associated morphology Enlargement true Inferred relationship Existential restriction modifier 1
Isolated congenital megalocornea Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Isolated congenital megalocornea Is a X-linked recessive hereditary disease true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start