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722019000: Oculootoradial syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3325063017 IVIC (Instituto Venezolano de Investigaciones Cientificas) syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3330144013 Oculootoradial syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3330145014 Oculootoradial syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3330146010 Oculo-oto-radial syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3330147018 IVIC syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Oculootoradial syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Oculootoradial syndrome Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Existential restriction modifier
Oculootoradial syndrome Is a Congenital anomaly of upper limb true Inferred relationship Existential restriction modifier
Oculootoradial syndrome Is a Congenital hearing disorder false Inferred relationship Existential restriction modifier
Oculootoradial syndrome Is a Dysostosis true Inferred relationship Existential restriction modifier
Oculootoradial syndrome Is a Finding of bone of upper limb true Inferred relationship Existential restriction modifier
Oculootoradial syndrome Is a Auditory system hereditary disorder true Inferred relationship Existential restriction modifier
Oculootoradial syndrome Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Oculootoradial syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Oculootoradial syndrome Finding site Structure of auditory system false Inferred relationship Existential restriction modifier 2
Oculootoradial syndrome Interprets Hearing, function true Inferred relationship Existential restriction modifier 3
Oculootoradial syndrome Interprets Functional observable false Inferred relationship Existential restriction modifier
Oculootoradial syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 4
Oculootoradial syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 4
Oculootoradial syndrome Finding site Bone structure of upper limb false Inferred relationship Existential restriction modifier 4
Oculootoradial syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Oculootoradial syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Oculootoradial syndrome Finding site Bone structure of upper limb true Inferred relationship Existential restriction modifier 1
Oculootoradial syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Oculootoradial syndrome Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
Oculootoradial syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Oculootoradial syndrome Is a Hearing loss associated with syndrome true Inferred relationship Existential restriction modifier
Oculootoradial syndrome Has interpretation Impaired true Inferred relationship Existential restriction modifier 3
Oculootoradial syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Oculootoradial syndrome Is a Mixed conductive and sensorineural hearing loss, bilateral true Inferred relationship Existential restriction modifier
Oculootoradial syndrome Is a Congenital mixed conductive and sensorineural hearing loss true Inferred relationship Existential restriction modifier
Oculootoradial syndrome Finding site Left ear structure true Inferred relationship Existential restriction modifier 4
Oculootoradial syndrome Finding site Right ear structure true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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