FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

405809000: Ocular motor apraxia Cogan type (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2004. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
2157583012 Oculomotor apraxia - Cogan type en Synonym Active Only initial character case insensitive SNOMED CT core module
5045004019 Ocular motor apraxia Cogan type (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
5045005018 Ocular motor apraxia Cogan type en Synonym Active Only initial character case insensitive SNOMED CT core module
5045006017 Congenital saccade initiation failure en Synonym Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Ocular motor apraxia Cogan type Is a Oculomotor apraxia true Inferred relationship Existential restriction modifier
Ocular motor apraxia Cogan type Finding site Eye region structure false Inferred relationship Existential restriction modifier 1
Ocular motor apraxia Cogan type Associated morphology Misalignment false Inferred relationship Existential restriction modifier 1
Ocular motor apraxia Cogan type Interprets Ocular muscle balance false Inferred relationship Existential restriction modifier 1
Ocular motor apraxia Cogan type Finding site Structure of visual system true Inferred relationship Existential restriction modifier 1
Ocular motor apraxia Cogan type Interprets Ocular motility observable false Inferred relationship Existential restriction modifier
Ocular motor apraxia Cogan type Has interpretation Abnormal false Inferred relationship Existential restriction modifier 1
Ocular motor apraxia Cogan type Interprets Ocular muscle balance false Inferred relationship Existential restriction modifier 1
Ocular motor apraxia Cogan type Has interpretation Abnormal false Inferred relationship Existential restriction modifier 1
Ocular motor apraxia Cogan type Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Ocular motor apraxia Cogan type Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Ocular motor apraxia Cogan type Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Ocular motor apraxia Cogan type Is a Congenital anomaly of visual system true Inferred relationship Existential restriction modifier
Ocular motor apraxia Cogan type Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Ocular motor apraxia Cogan type Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Ocular motor apraxia Cogan type Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Cortical paralysis of fixation syndrome Is a False Ocular motor apraxia Cogan type Inferred relationship Existential restriction modifier

This concept is not in any reference sets

Back to Start