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281300000: Below reference range (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
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

0 descendants.

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
Short stature with webbed neck and congenital heart disease syndrome (disorder) Has interpretation True Below reference range Inferred relationship Some 4
Short stature due to primary acid labile subunit deficiency (disorder) Has interpretation True Below reference range Inferred relationship Some 2
Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome (disorder) Has interpretation True Below reference range Inferred relationship Some 5
Hip dysplasia Beukes type (disorder) Has interpretation True Below reference range Inferred relationship Some 4
Hypogonadism with mitral valve prolapse and intellectual disability syndrome (disorder) Has interpretation True Below reference range Inferred relationship Some 4
Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome (disorder) Has interpretation True Below reference range Inferred relationship Some 6
Macrocephaly, short stature, paraplegia syndrome (disorder) Has interpretation True Below reference range Inferred relationship Some 8
Parastremmatic dwarfism (disorder) Has interpretation True Below reference range Inferred relationship Some 2
Congenital cataract, nephropathy, encephalopathy syndrome (disorder) Has interpretation True Below reference range Inferred relationship Some 4
Keratosis follicularis, dwarfism, cerebral atrophy syndrome Has interpretation True Below reference range Inferred relationship Some 5
Schimke immuno-osseous dysplasia (disorder) Has interpretation True Below reference range Inferred relationship Some 4
Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome (disorder) Has interpretation True Below reference range Inferred relationship Some 5
Microspherophakia with metaphyseal dysplasia syndrome (disorder) Has interpretation True Below reference range Inferred relationship Some 4
Microcephalic primordial dwarfism due to zinc finger protein 335 deficiency (disorder) Has interpretation True Below reference range Inferred relationship Some 2
Laron syndrome with immunodeficiency (disorder) Has interpretation True Below reference range Inferred relationship Some 3
Craniolenticulosutural dysplasia (disorder) Has interpretation True Below reference range Inferred relationship Some 4
Carbohydrate sulfotransferase 3 related skeletal dysplasia (disorder) Has interpretation True Below reference range Inferred relationship Some 5
Caudal appendage deafness syndrome (disorder) Has interpretation True Below reference range Inferred relationship Some 6
Short stature, unique facies, enamel hypoplasia, progressive joint stiffness, high-pitched voice syndrome (disorder) Has interpretation True Below reference range Inferred relationship Some 4
Short stature locking fingers syndrome (disorder) Has interpretation True Below reference range Inferred relationship Some 3
Coxoauricular syndrome (disorder) Has interpretation True Below reference range Inferred relationship Some 4
Dysmorphism, short stature, deafness, disorder of sex development syndrome Has interpretation True Below reference range Inferred relationship Some 5
Trigonocephaly, short stature, developmental delay syndrome (disorder) Has interpretation True Below reference range Inferred relationship Some 3
Deafness, vitiligo, achalasia syndrome Has interpretation True Below reference range Inferred relationship Some 6
Ichthyosis, intellectual disability, dwarfism, renal impairment syndrome (disorder) Has interpretation True Below reference range Inferred relationship Some 5
Ulna metaphyseal dysplasia syndrome (disorder) Has interpretation True Below reference range Inferred relationship Some 2
Skeletal dysplasia with epilepsy and short stature syndrome (disorder) Has interpretation True Below reference range Inferred relationship Some 2
Growth delay due to insulin-like growth factor I resistance (disorder) Has interpretation True Below reference range Inferred relationship Some 2
Multiple epiphyseal dysplasia type 4 (disorder) Has interpretation True Below reference range Inferred relationship Some 3
Multiple epiphyseal dysplasia type 1 (disorder) Has interpretation True Below reference range Inferred relationship Some 3
Multiple epiphyseal dysplasia type 5 (disorder) Has interpretation True Below reference range Inferred relationship Some 3
Cataract with aberrant oral frenula and growth delay syndrome (disorder) Has interpretation True Below reference range Inferred relationship Some 3
Goniodysgenesis with intellectual disability and short stature syndrome (disorder) Has interpretation True Below reference range Inferred relationship Some 2
Short stature with craniofacial anomalies and genital hypoplasia syndrome (disorder) Has interpretation True Below reference range Inferred relationship Some 4
Intellectual disability and short stature with hand contracture and genital anomaly syndrome (disorder) Has interpretation True Below reference range Inferred relationship Some 2
Autosomal dominant brachyolmia (disorder) Has interpretation True Below reference range Inferred relationship Some 2
Spondyloepimetaphyseal dysplasia Irapa type (disorder) Has interpretation True Below reference range Inferred relationship Some 2
Idiopathic short stature (disorder) Has interpretation True Below reference range Inferred relationship Some 2
Metaphyseal dysostosis, intellectual disability, conductive deafness syndrome Has interpretation True Below reference range Inferred relationship Some 4
Nutritional stunting in infancy (disorder) Has interpretation True Below reference range Inferred relationship Some 4
Nutritional stunting in childhood (disorder) Has interpretation True Below reference range Inferred relationship Some 4
Nutritional stunting in adolescence (disorder) Has interpretation True Below reference range Inferred relationship Some 4
KBG syndrome Has interpretation True Below reference range Inferred relationship Some 2
Short stature co-occurrent and due to endocrine disorder (disorder) Has interpretation True Below reference range Inferred relationship Some 4
Spondyloepimetaphyseal dysplasia Isidor type (disorder) Has interpretation True Below reference range Inferred relationship Some 2
Brachydactyly, short stature, retinitis pigmentosa syndrome (disorder) Has interpretation True Below reference range Inferred relationship Some 4
Richieri Costa-da Silva syndrome Has interpretation True Below reference range Inferred relationship Some 3
Thoracomelic dysplasia (disorder) Has interpretation True Below reference range Inferred relationship Some 3
Subaortic stenosis and short stature syndrome Has interpretation True Below reference range Inferred relationship Some 2
Short stature due to partial growth hormone receptor deficiency Has interpretation True Below reference range Inferred relationship Some 4
Ichthyosis, short stature, brachydactyly, microspherophakia syndrome Has interpretation True Below reference range Inferred relationship Some 6
Autosomal recessive brachyolmia (disorder) Has interpretation True Below reference range Inferred relationship Some 2
21q22.11q22.12 microdeletion syndrome Has interpretation True Below reference range Inferred relationship Some 4
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder) Has interpretation True Below reference range Inferred relationship Some 5
Autosomal recessive Robinow syndrome Has interpretation True Below reference range Inferred relationship Some 4
Osteogenesis imperfecta type 5 (disorder) Has interpretation True Below reference range Inferred relationship Some 3
Skeletal dysplasia, T-cell immunodeficiency, developmental delay syndrome (disorder) Has interpretation True Below reference range Inferred relationship Some 3
Congenital progressive bone marrow failure, B-cell immunodeficiency, skeletal dysplasia syndrome (disorder) Has interpretation True Below reference range Inferred relationship Some 3
Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome (disorder) Has interpretation True Below reference range Inferred relationship Some 4
Psychosocial short stature (disorder) Has interpretation True Below reference range Inferred relationship Some 2
Autosomal recessive brachyolmia and amelogenesis imperfecta syndrome (disorder) Has interpretation True Below reference range Inferred relationship Some 3
Short stature disorder due to osteosclerosis (disorder) Has interpretation True Below reference range Inferred relationship Some 3
Lethal congenital disproportionate short trunk short stature Has interpretation True Below reference range Inferred relationship Some 2
Lethal congenital disproportionate short limbed short stature (disorder) Has interpretation True Below reference range Inferred relationship Some 2
Intellectual disability, short stature, hypertelorism syndrome Has interpretation True Below reference range Inferred relationship Some 3
Pseudoleprechaunism syndrome Patterson type (disorder) Has interpretation True Below reference range Inferred relationship Some 4
Multiple epiphyseal dysplasia type 7 (disorder) Has interpretation True Below reference range Inferred relationship Some 3
Asymmetric short stature Has interpretation True Below reference range Inferred relationship Some 1
Infantile onset disproportionate short limb short stature Has interpretation True Below reference range Inferred relationship Some 2
Infantile onset disproportionate short trunk short stature Has interpretation True Below reference range Inferred relationship Some 2
Neonatal onset disproportionate short trunk short stature (disorder) Has interpretation True Below reference range Inferred relationship Some 2
Neonatal onset disproportionate short limb short stature Has interpretation True Below reference range Inferred relationship Some 2
Disproportionate short trunk short stature Has interpretation True Below reference range Inferred relationship Some 2
Disproportionate short limb short stature (disorder) Has interpretation True Below reference range Inferred relationship Some 2

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