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371880002: Abnormally low (qualifier value)

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

Descriptions:

Id Description Lang Type Status Case? Module
1197173014 Abnormally low (qualifier value) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1210470014 Abnormally low en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Abnormally low (qualifier value) Is a Low true Inferred relationship Some
Abnormally low (qualifier value) Is a Abnormal true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Hyporeflexia Has interpretation False Abnormally low (qualifier value) Inferred relationship Some 3
Decreased tendon reflex (finding) Has interpretation False Abnormally low (qualifier value) Inferred relationship Some 3
Diminished gastrin secretion Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 1
Hypotestosteronism Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 1
Feces pH more acidic than reference range (finding) Has interpretation False Abnormally low (qualifier value) Inferred relationship Some 1
Extracellular fluid volume depletion Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 1
Hypovolemia (finding) Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 1
Hyponatremia with extracellular fluid depletion Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 1
Absolute hypovolaemia Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 1
Relative hypovolemia (finding) Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 1
Gastrointestinal fluid volume depletion Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 1
Extrarenal fluid volume depletion Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 1
von Willebrand factor below reference range Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 1
Oesophagogastric junction outflow obstruction Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 2
Withdrawn behavior Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 1
Hereditary antithrombin III deficiency (disorder) Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 2
Acquired antithrombin III deficiency Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 1
Antithrombin III deficiency Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 2
Low birth weight infant Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 2
Very low birth weight infant Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 2
Extremely low birth weight infant Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 2
Hypotonia of muscle of upper limb Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 2
Poor muscle tone (finding) Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 2
Generalised hypotonia due to neuromuscular junction defect Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 4
Chloride voltage-gated channel 6-related childhood-onset progressive neurodegeneration, peripheral neuropathy syndrome (disorder) Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 6
Neonatal hypotonia Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 3
Traumatic hypotonia (disorder) Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 4
Benign congenital hypotonia Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 1
Cystinuria, type 1 Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 3
Flaccidity of muscle (finding) Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 2
Flaccidity of muscle of lower limb Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 2
Flaccidity of muscle of upper limb Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 2
Allan-Herndon-Dudley syndrome Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 9
Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 5
X-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behavior syndrome (disorder) Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 3
2p21 microdeletion syndrome (disorder) Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 6
Hypotonia cystinuria syndrome (disorder) Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 3
Puerto Rican infant hypotonia syndrome (disorder) Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 4
Acquired hypotonia Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 2
Atypical hypotonia cystinuria syndrome (disorder) Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 3
Multiple congenital anomalies, hypotonia, seizures syndrome (disorder) Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 4
Hypotonic-hyporesponsive episode (finding) Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 4
Intellectual disability, epilepsy, extrapyramidal syndrome Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 5
Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome (disorder) Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 5
Appendicular hypotonia Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 2
Episodic flaccidity of muscle (finding) Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 3
Episodic hypotonia Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 4
Hypotonia of axial muscles occurring in infancy Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 2
Hypotonia of muscles of mouth region (finding) Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 2
Hypotonia of muscle of face Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 2
Severe hypotonia of muscle (finding) Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 2
2p21 microdeletion syndrome without cystinuria (disorder) Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 8
Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome (disorder) Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 6
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 6
Intellectual disability, macrocephaly, hypotonia, behavioural abnormalities syndrome Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 8
Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome (disorder) Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 7
G protein subunit alpha o1-related developmental delay, seizures, movement disorder spectrum (disorder) Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 4
Neurodevelopmental delay, hypotonia, cerebellar ataxia, cardiac conduction defects syndrome Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 7
Lethal pontocerebellar hypoplasia, hypotonia, respiratory insufficiency syndrome Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 6
Congenital contracture of limbs and face, hypotonia, developmental delay syndrome Has interpretation True Abnormally low (qualifier value) Inferred relationship Some 7

Reference Sets

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