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783065004: Autosomal recessive optic atrophy type 7 (disorder)


Status: current, Not 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
3757317014 Autosomal recessive optic atrophy OPA7 type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3757318016 Autosomal recessive optic atrophy OPA7 (optic atrophy type 7) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3757319012 Autosomal recessive optic atrophy type 7 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3757320018 Autosomal recessive optic atrophy type 7 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3757321019 A rare syndromic hereditary optic neuropathy disorder with characteristics of early-onset severe progressive visual impairment, optic disc pallor and central scotoma, variably associated with dyschromatopsia, auditory neuropathy (for example mild progressive sensorineural hearing loss), sensorimotor axonal neuropathy and occasionally moderate hypertrophic cardiomyopathy. There is evidence the disease is caused by homozygous mutation in the TMEM126A gene on chromosome 11q1. 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
Autosomal recessive optic atrophy type 7 (disorder) localisation d'une constatation (attribut) Optic nerve structure true Inferred relationship Some 1
Autosomal recessive optic atrophy type 7 (disorder) est un(e) (attribut) Autosomal recessive hereditary disorder true Inferred relationship Some
Autosomal recessive optic atrophy type 7 (disorder) morphologie associée (attribut) Primary atrophy true Inferred relationship Some 1
Autosomal recessive optic atrophy type 7 (disorder) est un(e) (attribut) Hereditary optic atrophy true Inferred relationship Some
Autosomal recessive optic atrophy type 7 (disorder) est un(e) (attribut) Mitochondrial cytopathy true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Canada English language reference set (foundation metadata concept)

GB English

US English

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