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2667000: Absent (qualifier value)

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

Descriptions:

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
1820381000195115 assente it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
45821000188114 absence fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
88551000077110 absent fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
2282091000195117 Abwesend de Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

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
Motor level spinal weakness (finding) Has interpretation True Absent Inferred relationship Some 1
Spastic paralysis Has interpretation True Absent Inferred relationship Some 2
Pharyngeal paralysis Has interpretation True Absent Inferred relationship Some 1
Laryngeal hemiplegia Has interpretation True Absent Inferred relationship Some 1
Facial palsy as birth trauma Has interpretation False Absent Inferred relationship Some 3
Paralysis of larynx Has interpretation True Absent Inferred relationship Some 1
Ulnar neuropraxia Has interpretation True Absent Inferred relationship Some 2
à l'examen : paralysie Has interpretation False Absent Inferred relationship Some 1
à l'examen : paralysie du motoneurone supérieur du septième nerf crânien Has interpretation False Absent Inferred relationship Some 1
Bell's palsy Has interpretation True Absent Inferred relationship Some 1
Paresis of bilateral vocal cords (disorder) Has interpretation False Absent Inferred relationship Some 1
Bilateral total vocal cord paralysis Has interpretation False Absent Inferred relationship Some 1
Periodic paralysis Has interpretation True Absent Inferred relationship Some 1
Paralysis of glottis Has interpretation True Absent Inferred relationship Some 1
Congenital facial nerve palsy Has interpretation True Absent Inferred relationship Some 2
Familial facial nerve palsy Has interpretation True Absent Inferred relationship Some 1
Tourniquet palsy Has interpretation True Absent Inferred relationship Some 2
Congenital vocal cord palsy Has interpretation True Absent Inferred relationship Some 2
Acquired vocal cord palsy Has interpretation True Absent Inferred relationship Some 1
Paralysis following electric shock (finding) Has interpretation True Absent Inferred relationship Some 1
Transient limb paralysis Has interpretation True Absent Inferred relationship Some 1
Facial palsy (disorder) Has interpretation True Absent Inferred relationship Some 1
Vocal cord paralysis Has interpretation True Absent Inferred relationship Some 1
Tibial nerve palsy Has interpretation True Absent Inferred relationship Some 1
Ulnar nerve palsy Has interpretation True Absent Inferred relationship Some 2
Incomplete paralysis (finding) Has interpretation True Absent Inferred relationship Some 1
Peripheral facial palsy Has interpretation True Absent Inferred relationship Some 1
Acute flaccid paralysis (finding) Has interpretation True Absent Inferred relationship Some 1
Deafness-ear malformation-facial palsy syndrome is characterized by profound conductive deafness due to stapedial abnormalities associated with variable malformations of the external ears and facial paralysis. It has been described in three siblings and their mother. Inheritance is autosomal dominant. Has interpretation True Absent Inferred relationship Some 1
Congenital hereditary facial paralysis-variable hearing loss syndrome is an extremely rare autosomal recessive disorder characterized by bilateral facial palsy with masked facies, sensorineural hearing loss, dysmorphic features (midfacial retrusion, low-set ears), and strabismus. Has interpretation True Absent Inferred relationship Some 1
Acquired vocal cord paralysis in newborn (disorder) Has interpretation True Absent Inferred relationship Some 1
Mild dysfunction of the facial nerve evidenced by slight facial weakness, possible mild synkinesis, normal symmetry and tone at rest, moderate to good forehead movement, complete eye closure and slight asymmetry of the mouth. Has interpretation True Absent Inferred relationship Some 1
Moderate dysfunction of the facial nerve evidenced by asymmetry of the face without disfigurement, moderate synkinesis, contracture, or hemifacial spasm, normal symmetry and tone at rest, slight to moderate movement of forehead, complete eye closure with effort and slight weakness of the mouth which persists even with maximum effort. Has interpretation True Absent Inferred relationship Some 1
Moderately severe dysfunction of the facial nerve evidenced by weakness and/or asymmetry of the face causing disfigurement, normal symmetry and tone at rest, absence of forehead movement, incomplete eye closure and asymmetry of the mouth even with maximum effort. Has interpretation True Absent Inferred relationship Some 1
Severe dysfunction of the facial nerve evidenced by barely perceptible movement, facial asymmetry at rest, absence of forehead movement, incomplete eye closure, and only slight movement of the mouth. Has interpretation True Absent Inferred relationship Some 1
Total paralysis of the facial nerve. Has interpretation True Absent Inferred relationship Some 1
Musculocutaneous nerve palsy Has interpretation True Absent Inferred relationship Some 1
Tardy right ulnar nerve palsy Has interpretation True Absent Inferred relationship Some 3
Tardy left ulnar nerve palsy (finding) Has interpretation False Absent Inferred relationship Some 4
Numbness Has interpretation True Absent Inferred relationship Some 1
Glove anesthesia Has interpretation False Absent Inferred relationship Some 2
Numbness of tongue Has interpretation True Absent Inferred relationship Some 1
Perioral numbness Has interpretation True Absent Inferred relationship Some 1
Numbness of skin Has interpretation True Absent Inferred relationship Some 1
On examination - anesthesia in legs Has interpretation False Absent Inferred relationship Some 1
Numbness of vulva Has interpretation True Absent Inferred relationship Some 1
Numbness of upper limb Has interpretation True Absent Inferred relationship Some 1
Numbness of pinna Has interpretation True Absent Inferred relationship Some 1
Numbness of hand Has interpretation True Absent Inferred relationship Some 1
Numbness of finger Has interpretation True Absent Inferred relationship Some 1
Numbness of lower limb Has interpretation True Absent Inferred relationship Some 1
Numbness of foot Has interpretation True Absent Inferred relationship Some 1
Numbness of toe Has interpretation True Absent Inferred relationship Some 1
Numbness of face Has interpretation True Absent Inferred relationship Some 1
Numbness of limbs Has interpretation True Absent Inferred relationship Some 1
Numbness of saddle area Has interpretation True Absent Inferred relationship Some 1
Numbness and tingling sensation of skin Has interpretation True Absent Inferred relationship Some 1
Severe pediatric obstructive sleep apnea (disorder) Has interpretation True Absent Inferred relationship Some 3
A rare syndromic neurological disorder characterized by the association of Möbius syndrome (congenital facial palsy with impaired ocular abduction) with peripheral axonal neuropathy and hypogonadotropic hypogonadism. There have been no further reports since 1996. Has interpretation True Absent Inferred relationship Some 5
Isolated hereditary congenital facial paralysis (IHCFP) is an extremely rare neurological disorder presumed to result from maldevelopment of the facial nucleus and/or cranial nerve and has been reported in fewer than 10 families to date. It manifests as non-progressive, isolated, unilateral or bilateral, symmetrical or asymmetrical facial palsy. Involvement of the branches of the facial nerve can be unequal. Has interpretation True Absent Inferred relationship Some 2
Flaccid monoplegia of upper limb (disorder) Has interpretation True Absent Inferred relationship Some 1
Flaccid monoplegia of lower limb (disorder) Has interpretation True Absent Inferred relationship Some 1
Edentulous Has interpretation True Absent Inferred relationship Some 1
Edentulous maxillomandibular relationship class I Has interpretation True Absent Inferred relationship Some 1
Edentulous maxillomandibular relationship class II (finding) Has interpretation True Absent Inferred relationship Some 1
Edentulous maxillomandibular relationship class III (finding) Has interpretation True Absent Inferred relationship Some 1
Senile anodontia Has interpretation False Absent Inferred relationship Some 2
Right common peroneal nerve palsy Has interpretation True Absent Inferred relationship Some 2
Left common peroneal nerve palsy Has interpretation True Absent Inferred relationship Some 2
Paralysis of right radial nerve (finding) Has interpretation True Absent Inferred relationship Some 2
Paralysis of left radial nerve (finding) Has interpretation True Absent Inferred relationship Some 2
Heat exhaustion co-occurrent and due to anhidrosis (disorder) Has interpretation True Absent Inferred relationship Some 5
Acquired generalized anorgasmia (disorder) Has interpretation True Absent Inferred relationship Some 3
Acquired situational anorgasmia (disorder) Has interpretation True Absent Inferred relationship Some 3
Lifelong generalized anorgasmia (disorder) Has interpretation True Absent Inferred relationship Some 3
Lifelong situational anorgasmia (disorder) Has interpretation True Absent Inferred relationship Some 3
No epigastric sounds (finding) Has interpretation True Absent Inferred relationship Some 2
Mixed neonatal apnoea Has interpretation False Absent Inferred relationship Some 7
Primary physiologic amenorrhea Has interpretation True Absent Inferred relationship Some 1
Amenorrhea Has interpretation True Absent Inferred relationship Some 1
Dysponderal amenorrhea Has interpretation True Absent Inferred relationship Some 1
Premenopausal amenorrhea Has interpretation True Absent Inferred relationship Some 1
Physiologic amenorrhea Has interpretation True Absent Inferred relationship Some 1
Pathologic amenorrhea Has interpretation True Absent Inferred relationship Some 1
Dietary amenorrhea Has interpretation True Absent Inferred relationship Some 1
Cryptomenorrhea Has interpretation True Absent Inferred relationship Some 1
Non-pregnancy related A-G syndrome Has interpretation True Absent Inferred relationship Some 1
Postpartum amenorrhoea-galactorrhea syndrome Has interpretation False Absent Inferred relationship Some 1
Secondary physiologic amenorrhea Has interpretation True Absent Inferred relationship Some 1
Exercise-related amenorrhoea Has interpretation True Absent Inferred relationship Some 1
Lactational amenorrhoea Has interpretation True Absent Inferred relationship Some 1
Amenorrhea associated with obesity (finding) Has interpretation True Absent Inferred relationship Some 1
Anovulatory amenorrhea (finding) Has interpretation True Absent Inferred relationship Some 1
Normogonadotropic amenorrhea (finding) Has interpretation True Absent Inferred relationship Some 1
Gastroesophageal reflux disease with apnea (disorder) Has interpretation True Absent Inferred relationship Some 1
Aperistalsis of esophagus Has interpretation True Absent Inferred relationship Some 1
Paralysis of right vocal cord Has interpretation True Absent Inferred relationship Some 1
Paralysis of left vocal cord (disorder) Has interpretation True Absent Inferred relationship Some 1
A rare neurologic disorder characterized by a unique non-REM and REM parasomnia with sleep breathing dysfunction, gait instability and repetitive episodes of respiratory insufficiency, as well as autoantibodies against IgLON5. Patients may present stridor, chorea, limb ataxia, abnormal ocular movements, and bulbar symptoms (i.e. dysphagia, dysarthria, episodic central hypoventilation) with normal brain MRI. Excessive day sleepiness and cognitive deterioration have also been reported. Has interpretation True Absent Inferred relationship Some 3
A very rare congenital cranial dysinnervation disorder characterised by unilateral or bilateral non progressive congenital facial palsy (VII cranial nerve) with impairments of ocular abduction (VI cranial nerve). It can also be associated with other cranial nerves palsies, orofacial anomalies and limb defects. Has interpretation True Absent Inferred relationship Some 1
No cough strength Has interpretation True Absent Inferred relationship Some 1

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