281300000: onder referentiebereik (kwalificatiewaarde)

SNOMED CT Concept\Qualifier value\Finding value (qualifier value)\...

\Interpretation value\Reference range interpretation value\Outside reference range (qualifier value)\Below reference range

\Finding status values\Change values\Changed status (qualifier value)\Decreased\Below reference range

\Degree findings\Decreased\Below reference range

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
Below reference range	Is a	Reference range comments	false	Inferred relationship	Some
Below reference range	Is a	Outside reference range (qualifier value)	true	Inferred relationship	Some
Below reference range	Is a	Decreased	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
PYCR2-related microcephaly, progressive leucoencephalopathy	Has interpretation	True	Below reference range	Inferred relationship	Some	4
NDE1-related microhydranencephaly	Has interpretation	True	Below reference range	Inferred relationship	Some	5
Cerebellar-facial-dental syndrome (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	5
Short stature, developmental delay, congenital heart defect syndrome	Has interpretation	True	Below reference range	Inferred relationship	Some	4
Coffin-Lowry syndrome	Has interpretation	True	Below reference range	Inferred relationship	Some	6
Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	5
Fatty acyl-coenzyme A reductase 1 deficiency (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	3
Fatty acyl-coenzyme A reductase 1 deficiency (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	6
Warts, hypogammaglobulinaemia, infections, and myelokathexis	Has interpretation	True	Below reference range	Inferred relationship	Some	2
USP18 deficiency	Has interpretation	True	Below reference range	Inferred relationship	Some	3
Beta-1,3-galactosyltransferase 6-related spondylodysplastic Ehlers-Danlos syndrome (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	5
Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	8
Classical-like Ehlers-Danlos syndrome type 2	Has interpretation	True	Below reference range	Inferred relationship	Some	5
Oculocerebrodental syndrome	Has interpretation	True	Below reference range	Inferred relationship	Some	6
X-linked intellectual disability, short stature, overweight syndrome	Has interpretation	True	Below reference range	Inferred relationship	Some	5
Upshaw-Schulman syndrome (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	5
Hypoxic nephrosis	Has interpretation	True	Below reference range	Inferred relationship	Some	1
Hypocomplementaemic urticarial vasculitis	Has interpretation	True	Below reference range	Inferred relationship	Some	3
von Willebrand factor below reference range	Has interpretation	True	Below reference range	Inferred relationship	Some	2
Hypoglobulinaemia	Has interpretation	True	Below reference range	Inferred relationship	Some	1
Decreased renal clearance	Has interpretation	True	Below reference range	Inferred relationship	Some	2
Menke Hennekam syndrome	Has interpretation	True	Below reference range	Inferred relationship	Some	4
Menke Hennekam syndrome	Has interpretation	True	Below reference range	Inferred relationship	Some	5
Wasting syndrome due to acquired immunodeficiency syndrome (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	3
Idiopathic steroid-resistant nephrotic syndrome (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	1
Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance	Has interpretation	True	Below reference range	Inferred relationship	Some	3
Hematopoietic subsyndrome of acute radiation syndrome (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	4
Hematopoietic subsyndrome of acute radiation syndrome (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	5
Hematopoietic subsyndrome of acute radiation syndrome (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	6
Hematopoietic subsyndrome of acute radiation syndrome (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	7
Rhizomelic dysplasia (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	2
Robinow syndrome	Has interpretation	True	Below reference range	Inferred relationship	Some	6
Langer mesomelic dysplasia syndrome	Has interpretation	True	Below reference range	Inferred relationship	Some	3
Nievergelt's syndrome	Has interpretation	True	Below reference range	Inferred relationship	Some	3
Leri-Weill dyschondrosteosis	Has interpretation	True	Below reference range	Inferred relationship	Some	3
Mesomelic dysplasia	Has interpretation	True	Below reference range	Inferred relationship	Some	2
Rhizomelic syndrome Urbach type	Has interpretation	True	Below reference range	Inferred relationship	Some	2
Colobomatous microphthalmia, rhizomelic dysplasia syndrome (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	3
Mesomelic dysplasia Kantaputra type (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	2
Cleidorhizomelic syndrome (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	2
syndroom van dyschondrosteose en nefritis	Has interpretation	False	Below reference range	Inferred relationship	Some	3
Mesomelic dysplasia with cleft palate and camptodactyly syndrome (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	4
Mesomelic dysplasia of hypoplastic ulna and fibula type (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	2
Thoracic dysplasia and hydrocephalus syndrome	Has interpretation	True	Below reference range	Inferred relationship	Some	4
Autosomal recessive Robinow syndrome	Has interpretation	True	Below reference range	Inferred relationship	Some	6
Autosomal dominant Robinow syndrome (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	6
Leri-Weill dyschondrosteosis	Has interpretation	True	Below reference range	Inferred relationship	Some	8
Mesomelic dysplasia of upper limb (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	3
Mesomelic dysplasia of upper limb (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	4
Mesomelic dysplasia of lower limb	Has interpretation	True	Below reference range	Inferred relationship	Some	3
Mesomelic dysplasia of lower limb	Has interpretation	True	Below reference range	Inferred relationship	Some	4
Brachydactyly, mesomelia, intellectual disability, heart defect syndrome (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	6
Brachydactyly, mesomelia, intellectual disability, heart defect syndrome (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	9
SHOX-related short stature	Has interpretation	True	Below reference range	Inferred relationship	Some	2
Mesomelic dysplasia Kantaputra type (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	5
Mesomelic dysplasia Savarirayan type (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	5
Mesomelic dysplasia Savarirayan type (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	6
Mesomelic dysplasia of hypoplastic ulna and fibula type (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	4
Diastrophic dysplasia	Has interpretation	True	Below reference range	Inferred relationship	Some	5
Autosomal recessive Robinow syndrome	Has interpretation	True	Below reference range	Inferred relationship	Some	8
Congenital hypoplasia of ulna and intellectual disability syndrome (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	5
Brachydactyly type A6 (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	3
X-linked spondyloepimetaphyseal dysplasia (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	2
X-linked spondyloepimetaphyseal dysplasia (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	3
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	3
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	4
Axial spondylometaphyseal dysplasia (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	2
Multiple epiphyseal dysplasia Lowry type (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	5
Spondyloepimetaphyseal dysplasia, hypotrichosis syndrome	Has interpretation	True	Below reference range	Inferred relationship	Some	4
Omodysplasia (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	2
Autosomal dominant omodysplasia (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	2
Autosomal recessive omodysplasia (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	2
Bone dysplasia lethal Holmgren type (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	2
Rhizomelic dysplasia of Patterson Lowry type (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	2
Rhizomelic dysplasia of Patterson Lowry type (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	3
Smith McCort dysplasia (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	3
Autosomal recessive spondylometaphyseal dysplasia Megarbane type (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	2
Regressive spondylometaphyseal dysplasia	Has interpretation	True	Below reference range	Inferred relationship	Some	2
Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	7
Spondyloepimetaphyseal dysplasia, hypotrichosis syndrome	Has interpretation	True	Below reference range	Inferred relationship	Some	3
Smith McCort dysplasia (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	2
Cleidorhizomelic syndrome (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	4
Autosomal recessive spondylometaphyseal dysplasia Megarbane type (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	3
Multiple epiphyseal dysplasia Lowry type (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	3
Autosomal dominant osteopetrosis type 1	Has interpretation	True	Below reference range	Inferred relationship	Some	2
Distal arthrogryposis type 3 (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	4
Familial lecithin cholesterol acyltransferase deficiency (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	2
Lecithin cholesterol acyltransferase deficiency	Has interpretation	True	Below reference range	Inferred relationship	Some	2
Fish-eye disease	Has interpretation	True	Below reference range	Inferred relationship	Some	1
Hyponatremia	Has interpretation	True	Below reference range	Inferred relationship	Some	1
Hyponatremia with excess extracellular fluid volume	Has interpretation	True	Below reference range	Inferred relationship	Some	1
Water intoxication syndrome	Has interpretation	True	Below reference range	Inferred relationship	Some	2
Hyponatremia with normal extracellular fluid volume	Has interpretation	True	Below reference range	Inferred relationship	Some	1
Cerebral hyponatremia	Has interpretation	True	Below reference range	Inferred relationship	Some	3
Chronic hyponatremia	Has interpretation	True	Below reference range	Inferred relationship	Some	2
Hyponatremia with decreased serum osmolality	Has interpretation	True	Below reference range	Inferred relationship	Some	1
Transurethral resection of prostate (TURP) syndrome	Has interpretation	True	Below reference range	Inferred relationship	Some	3
Dilutional hyponatremia	Has interpretation	True	Below reference range	Inferred relationship	Some	1
Acute hyponatremia	Has interpretation	True	Below reference range	Inferred relationship	Some	1
Transitory neonatal hyponatraemia	Has interpretation	True	Below reference range	Inferred relationship	Some	3
Paraneoplastic hyponatremia (disorder)	Has interpretation	True	Below reference range	Inferred relationship	Some	1

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Id	Description	Lang	Type	Status	Case?	Module
419283014	Below reference range	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
674819018	Below reference range (qualifier value)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4190321000146112	onder referentiebereik	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
4190331000146114	onder referentiebereik (kwalificatiewaarde)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
4190341000146118	verlaagd	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
4260731000146111	onder referentie-interval	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)