FHIR © HL7.org | Server Home | FHIR Server FHIR Server 3.7.10 | FHIR Version n/a User: [n/a]

2667000: Absent (qualifier value)

SNOMED CT Concept\Qualifier value\Finding value (qualifier value)\Absence findings\Absent

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Absent	Is a	General adjectival modifier	false	Inferred relationship	Some
Absent	Is a	Absence findings	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Lethal neonatal spasticity, epileptic encephalopathy syndrome (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	4
Acquired horizontal gaze palsy (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	4
Ophthalmoplegia due to abetalipoproteinemia (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	5
Isolated acquired horizontal gaze palsy (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	4
Congenital fibrosis syndrome (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	4
Congenital horizontal gaze palsy (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	3
Isolated congenital horizontal gaze paresis	Has interpretation	True	Absent	Inferred relationship	Some	4
Intermittent horizontal conjugate gaze deviation (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	6
Intermittent upward gaze deviation (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	6
Horizontal gaze preference (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	3
Ophthalmoplegia due to and following Guillain-Barré syndrome (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	5
Ophthalmoplegia due to neuropathy (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	4
Paralysis of downgaze	Has interpretation	True	Absent	Inferred relationship	Some	4
Paralysis of upgaze (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	4
Combined paralysis of upgaze and downgaze	Has interpretation	True	Absent	Inferred relationship	Some	4
Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome	Has interpretation	True	Absent	Inferred relationship	Some	1
Wall-eyed bilateral internuclear ophthalmoplegia syndrome (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	4
Absence of placental secretion of chorionic gonadotropin	Has interpretation	True	Absent	Inferred relationship	Some	2
Intellectual disability, spasticity, ectrodactyly syndrome	Has interpretation	True	Absent	Inferred relationship	Some	9
Macrocephaly, short stature, paraplegia syndrome (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	13
Severe microbrachycephaly, intellectual disability, athetoid cerebral palsy syndrome	Has interpretation	True	Absent	Inferred relationship	Some	9
Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	9
Congenital ichthyosis, intellectual disability, spastic quadriplegia syndrome (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	7
NK6 homeobox 2-related autosomal recessive hypomyelinating leukodystrophy (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	11
Hypotonic cerebral palsy	Has interpretation	True	Absent	Inferred relationship	Some	5
Allan-Herndon-Dudley syndrome	Has interpretation	True	Absent	Inferred relationship	Some	11
Pseudoprogeria syndrome (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	9
Spastic paraplegia, glaucoma, intellectual disability syndrome	Has interpretation	True	Absent	Inferred relationship	Some	10
Tardy left ulnar nerve palsy (finding)	Has interpretation	True	Absent	Inferred relationship	Some	2
Ophthalmoplegia, intellectual disability, lingua scrotalis syndrome (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	7
Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome	Has interpretation	True	Absent	Inferred relationship	Some	10
Spastic paraplegia, severe developmental delay, epilepsy syndrome	Has interpretation	True	Absent	Inferred relationship	Some	10
Severe oculo-renal-cerebellar syndrome (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	10
Vertical one-and-a-half syndrome (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	4
Periodic alternating gaze deviation	Has interpretation	True	Absent	Inferred relationship	Some	4
Ophthalmoplegia due to phytanic acid storage disease (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	4
Sustained upward gaze deviation (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	4
Sustained horizontal conjugate gaze deviation, contralateral type (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	5
Sustained horizontal conjugate gaze deviation, ipsilateral type (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	5
Sustained horizontal conjugate gaze deviation	Has interpretation	True	Absent	Inferred relationship	Some	5
Paralytic shellfish poisoning	Has interpretation	True	Absent	Inferred relationship	Some	1
Hypothalamic adipsic hypernatremia syndrome (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	2
Traumatic loss of tooth	Has interpretation	True	Absent	Inferred relationship	Some	3
Autosomal dominant complex hereditary spastic paraplegia (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	2
Congenital multi-minicore disease with external ophthalmoplegia (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	3
Spastic paraplegia, intellectual disability, nystagmus, obesity syndrome	Has interpretation	True	Absent	Inferred relationship	Some	11
Andersen Tawil syndrome (disorder)	Has interpretation	True	Absent	Inferred relationship	Some	1
Congenital insensitivity to pain, anosmia, neuropathic arthropathy	Has interpretation	True	Absent	Inferred relationship	Some	2
No active range of ankle dorsiflexion (finding)	Has interpretation	True	Absent	Inferred relationship	Some	1
No passive range of ankle dorsiflexion (finding)	Has interpretation	True	Absent	Inferred relationship	Some	1
No passive range of ankle plantar flexion	Has interpretation	True	Absent	Inferred relationship	Some	1
No active range of ankle plantar flexion (finding)	Has interpretation	True	Absent	Inferred relationship	Some	1
Tooth unerupted	Has interpretation	True	Absent	Inferred relationship	Some	2

Start Previous Page 13 of 13

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
5527017	Absent	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5528010	Absence of	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
757146018	Absent (qualifier value)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
7369261000172112	afwezigheid van	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
7369271000172115	afwezig	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)