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771336003: Polymicrogyria with optic nerve hypoplasia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3705808010 Polymicrogyria with optic nerve hypoplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3705809019 Polymicrogyria with optic nerve hypoplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3705810012 A rare genetic syndrome with characteristics of severe developmental delay, neonatal hypotonia, seizures, optic nerve hypoplasia and distinct central nervous system malformations including extensive bilateral polymicrogyria, dysplastic or absent corpus callosum and malformed brainstem with loss of demarcation of the pontomedullary junction. There is evidence this disease is caused by homozygous mutation in the TUBA8 gene on chromosome 22q11. 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
Polymicrogyria with optic nerve hypoplasia Is a Hypoplasia of the optic nerve true Inferred relationship Some
Polymicrogyria with optic nerve hypoplasia Occurrence Congenital true Inferred relationship Some 2
Polymicrogyria with optic nerve hypoplasia Is a Intellectual disability true Inferred relationship Some
Polymicrogyria with optic nerve hypoplasia Is a Hereditary disorder of nervous system false Inferred relationship Some
Polymicrogyria with optic nerve hypoplasia Is a Hereditary disorder of the visual system (disorder) false Inferred relationship Some
Polymicrogyria with optic nerve hypoplasia Associated morphology Congenital smallness false Inferred relationship Some 2
Polymicrogyria with optic nerve hypoplasia Is a Bilateral polymicrogyria (disorder) true Inferred relationship Some
Polymicrogyria with optic nerve hypoplasia Finding site Structure of gyrus of brain (body structure) true Inferred relationship Some 2
Polymicrogyria with optic nerve hypoplasia Finding site Optic nerve structure true Inferred relationship Some 1
Polymicrogyria with optic nerve hypoplasia Associated morphology Hypoplasia true Inferred relationship Some 1
Polymicrogyria with optic nerve hypoplasia Occurrence Congenital true Inferred relationship Some 1
Polymicrogyria with optic nerve hypoplasia Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Polymicrogyria with optic nerve hypoplasia Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Polymicrogyria with optic nerve hypoplasia Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Polymicrogyria with optic nerve hypoplasia Is a Inherited optic neuropathy true Inferred relationship Some
Polymicrogyria with optic nerve hypoplasia Is a Developmental hereditary disorder true Inferred relationship Some
Polymicrogyria with optic nerve hypoplasia Interprets Intellectual ability (observable entity) true Inferred relationship Some 3
Polymicrogyria with optic nerve hypoplasia Has interpretation Impaired true Inferred relationship Some 3
Polymicrogyria with optic nerve hypoplasia Interprets Adaptation behavior (observable entity) true Inferred relationship Some 4
Polymicrogyria with optic nerve hypoplasia Has interpretation Impaired true Inferred relationship Some 4
Polymicrogyria with optic nerve hypoplasia Associated morphology Abnormal smallness (morphologic abnormality) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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