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1230016009: Familial congenital nasolacrimal duct obstruction (disorder)


Status: current, Defined. Date: 31-May 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5066409018 Familial congenital nasolacrimal duct obstruction (disorder) en Fully specified name Active Case insensitive SNOMED CT core
5066410011 Familial congenital nasolacrimal duct obstruction en Synonym Active Case insensitive SNOMED CT core
5066411010 A rare genetic otorhinolaryngological malformation with characteristics of congenital impatency of the nasolacrimal drainage system in various members of a family. Presentation is not specific and may include a uni or bilateral medial canthal mass, dacryocystitis, nasal obstruction, periorbital cellulitis and epiphora. Dacryocystocele and lacrimal puncta agenesis may be associated. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial congenital nasolacrimal duct obstruction Is a Familial disease true Inferred relationship Some
Familial congenital nasolacrimal duct obstruction Is a Congenital nasolacrimal duct obstruction true Inferred relationship Some
Familial congenital nasolacrimal duct obstruction Is a Developmental hereditary disorder true Inferred relationship Some
Familial congenital nasolacrimal duct obstruction Is a Hereditary disorder of the visual system true Inferred relationship Some
Familial congenital nasolacrimal duct obstruction Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Familial congenital nasolacrimal duct obstruction Occurrence Congenital true Inferred relationship Some 1
Familial congenital nasolacrimal duct obstruction Finding site Nasolacrimal duct structure true Inferred relationship Some 1
Familial congenital nasolacrimal duct obstruction Associated morphology Obstruction true Inferred relationship Some 1
Familial congenital nasolacrimal duct obstruction Pathological process Pathological developmental process true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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