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770944002: Oculootodental syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3703553016 Oculootodental syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3703555011 Oculootodental syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Oculootodental syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Oculootodental syndrome Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 1
Oculootodental syndrome Is a Globodontia true Inferred relationship Existential restriction modifier
Oculootodental syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Oculootodental syndrome Is a Congenital sensorineural hearing loss true Inferred relationship Existential restriction modifier
Oculootodental syndrome Finding site Chromosome pair 11 true Inferred relationship Existential restriction modifier 1
Oculootodental syndrome Is a Hearing loss associated with syndrome true Inferred relationship Existential restriction modifier
Oculootodental syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 4
Oculootodental syndrome Finding site Long arm of chromosome true Inferred relationship Existential restriction modifier 2
Oculootodental syndrome Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 2
Oculootodental syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Oculootodental syndrome Interprets Hearing, function true Inferred relationship Existential restriction modifier 5
Oculootodental syndrome Is a Deletion of part of chromosome 11 true Inferred relationship Existential restriction modifier
Oculootodental syndrome Associated morphology Congenital enlargement false Inferred relationship Existential restriction modifier 4
Oculootodental syndrome Finding site Ear structure true Inferred relationship Existential restriction modifier 3
Oculootodental syndrome Finding site Tooth structure true Inferred relationship Existential restriction modifier 4
Oculootodental syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Oculootodental syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Oculootodental syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Oculootodental syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 4
Oculootodental syndrome Associated morphology Enlargement true Inferred relationship Existential restriction modifier 4
Oculootodental syndrome Is a Disorder of ear true Inferred relationship Existential restriction modifier
Oculootodental syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 6
Oculootodental syndrome Finding site Tooth structure false Inferred relationship Existential restriction modifier 6
Oculootodental syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 6
Oculootodental syndrome Is a Congenital malformation true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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