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1303582008: Congenital aphakia, iris hypoplasia, microphthalmia, microcornea syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Mar 2024. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5307034013 Congenital aphakia, iris hypoplasia, microphthalmia, microcornea syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5307035014 Congenital aphakia, iris hypoplasia, microphthalmia, microcornea syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5307036010 A rare genetic disorder involving multiple structures of the eye. The disease is characterised by a combination of congenital aphakia and pan ocular anomalies including iris hypoplasia, microphthalmia, and microcornea. Other ophthalmological features may include nystagmus, glaucoma, strabismus, congenital leukocoria, anterior persistent fetal vasculature and posterior segment anomalies (e.g. optic nerve and foveal hypoplasia, intravitreous haemorrhages). No extraocular manifestations are observed. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5307037018 A rare genetic disorder involving multiple structures of the eye. The disease is characterized by a combination of congenital aphakia and pan ocular anomalies including iris hypoplasia, microphthalmia, and microcornea. Other ophthalmological features may include nystagmus, glaucoma, strabismus, congenital leukocoria, anterior persistent fetal vasculature and posterior segment anomalies (e.g. optic nerve and foveal hypoplasia, intravitreous hemorrhages). No extraocular manifestations are observed. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital aphakia, iris hypoplasia, microphthalmia, microcornea syndrome Is a Congenital aphakia true Inferred relationship Some
Congenital aphakia, iris hypoplasia, microphthalmia, microcornea syndrome Is a Genetic disease true Inferred relationship Some
Congenital aphakia, iris hypoplasia, microphthalmia, microcornea syndrome Occurrence Congenital true Inferred relationship Some 1
Congenital aphakia, iris hypoplasia, microphthalmia, microcornea syndrome Finding site Entire lens true Inferred relationship Some 1
Congenital aphakia, iris hypoplasia, microphthalmia, microcornea syndrome Associated morphology Agenesis (morphologic abnormality) true Inferred relationship Some 1
Congenital aphakia, iris hypoplasia, microphthalmia, microcornea syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital aphakia, iris hypoplasia, microphthalmia, microcornea syndrome Is a Congenital malformation syndrome (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

GB English

US English

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