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399120006: Infantile cataract (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1767040019 Infantile cataract (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1778580018 Infantile cataract en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5256661000241113 cataracte infantile fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
524811000274112 Infantile Katarakt de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Infantile cataract (disorder) Is a Nonsenile cataract (disorder) true Inferred relationship Some
Infantile cataract (disorder) Associated morphology Abnormally opaque structure (morphologic abnormality) true Inferred relationship Some 1
Infantile cataract (disorder) Finding site Lens clear true Inferred relationship Some 1
Infantile cataract (disorder) Associated morphology Abnormally opaque structure (morphologic abnormality) false Inferred relationship Some 1
Infantile cataract (disorder) Finding site Lens clear false Inferred relationship Some 1
Infantile cataract (disorder) Associated morphology Cataract false Inferred relationship Some 2
Infantile cataract (disorder) Finding site Lens clear false Inferred relationship Some 2
Infantile cataract (disorder) Is a Infantile and/or juvenile cataract true Inferred relationship Some
Infantile cataract (disorder) Occurrence Infancy true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome is characterized by congenital muscular dystrophy, infantile cataract and hypogonadism. It has been described in seven individuals from an isolated Norwegian village and in one unrelated individual. Transmission appears to be autosomal recessive. Is a True Infantile cataract (disorder) Inferred relationship Some

This concept is not in any reference sets

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