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1250004: Decreased (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
3205012 Decreased en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3206013 Diminished en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3207016 Decreased by en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
728771012 Decreased (qualifier value) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
88541000077112 diminué fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Decreased Is a Degree findings true Inferred relationship Some
Decreased Is a General adjectival modifier false Inferred relationship Some
Decreased Is a Changed status (qualifier value) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome (disorder) Has interpretation True Decreased Inferred relationship Some 2
Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome (disorder) Has interpretation True Decreased Inferred relationship Some 3
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) Has interpretation True Decreased Inferred relationship Some 4
Spondyloepiphyseal dysplasia Stanescu type Has interpretation True Decreased Inferred relationship Some 4
Decreased amniotic fluid production Has interpretation True Decreased Inferred relationship Some 1
PCNA-related progressive neurodegenerative photosensitivity syndrome Has interpretation True Decreased Inferred relationship Some 2
Bilateral hypotony of eyes due to ocular fistula Has interpretation True Decreased Inferred relationship Some 3
Hypotony of left eye due to ocular fistula (disorder) Has interpretation True Decreased Inferred relationship Some 2
Hypotony of right eye due to ocular fistula Has interpretation True Decreased Inferred relationship Some 2
Loss of subcutaneous fat Has interpretation True Decreased Inferred relationship Some 2
Loss of subcutaneous fat overlying biceps muscle (finding) Has interpretation True Decreased Inferred relationship Some 3
Loss of subcutaneous fat overlying triceps muscle (finding) Has interpretation True Decreased Inferred relationship Some 3
Loss of subcutaneous fat overlying rib (finding) Has interpretation True Decreased Inferred relationship Some 3
Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome (disorder) Has interpretation True Decreased Inferred relationship Some 4
Duane retraction syndrome with congenital deafness Has interpretation True Decreased Inferred relationship Some 4
Postpartum afibrinogenemia with hemorrhage Has interpretation True Decreased Inferred relationship Some 4
Deafness, enamel hypoplasia, nail defect syndrome (disorder) Has interpretation True Decreased Inferred relationship Some 5
Psychogenic syncope (disorder) Has interpretation True Decreased Inferred relationship Some 1
Psychogenic syncope (disorder) Has interpretation True Decreased Inferred relationship Some 2
Congenital cochleovestibular malformation Has interpretation True Decreased Inferred relationship Some 2
Alstrom syndrome Has interpretation True Decreased Inferred relationship Some 4
Xeroderma of eyelid Has interpretation True Decreased Inferred relationship Some 1
Xeroderma Has interpretation True Decreased Inferred relationship Some 1
Pigmented xerodermoid Has interpretation False Decreased Inferred relationship Some 1
Xeroderma pigmentosum, group D Has interpretation True Decreased Inferred relationship Some 1
Xeroderma pigmentosum, variant form Has interpretation True Decreased Inferred relationship Some 1
Xeroderma pigmentosum, group E Has interpretation True Decreased Inferred relationship Some 1
Xeroderma pigmentosum, group G Has interpretation True Decreased Inferred relationship Some 1
Xeroderma pigmentosum, group F Has interpretation True Decreased Inferred relationship Some 1
Xeroderma pigmentosum, group A Has interpretation True Decreased Inferred relationship Some 1
Xeroderma pigmentosum Has interpretation True Decreased Inferred relationship Some 2
Xeroderma pigmentosum, group C (disorder) Has interpretation True Decreased Inferred relationship Some 1
Vitamin A deficiency with xeroderma Has interpretation True Decreased Inferred relationship Some 2
XTE syndrome Has interpretation True Decreased Inferred relationship Some 2
Non-neurologic xeroderma pigmentosum Has interpretation True Decreased Inferred relationship Some 1
Xeroderma pigmentosum, group B Has interpretation True Decreased Inferred relationship Some 1
Senile xeroderma Has interpretation True Decreased Inferred relationship Some 1
Drug-induced ichthyosiform reaction Has interpretation True Decreased Inferred relationship Some 4
Dry skin dermatitis Has interpretation True Decreased Inferred relationship Some 3
Xeroderma in genetic syndrome (disorder) Has interpretation True Decreased Inferred relationship Some 1
Xerosis due to atopic dermatitis (disorder) Has interpretation True Decreased Inferred relationship Some 2
Xeroderma of left eyelid Has interpretation True Decreased Inferred relationship Some 3
Xeroderma of right eyelid (disorder) Has interpretation True Decreased Inferred relationship Some 3
Xeroderma of right upper eyelid Has interpretation True Decreased Inferred relationship Some 3
Xeroderma of left upper eyelid Has interpretation True Decreased Inferred relationship Some 3
Xeroderma of lower eyelid Has interpretation True Decreased Inferred relationship Some 1
Xeroderma of upper eyelid Has interpretation True Decreased Inferred relationship Some 2
Severe dry skin Has interpretation True Decreased Inferred relationship Some 2
Trichodysplasia xeroderma syndrome (disorder) Has interpretation True Decreased Inferred relationship Some 1
Dry skin of abdomen Has interpretation True Decreased Inferred relationship Some 2
Xeroderma pigmentosum and Cockayne syndrome complex (disorder) Has interpretation True Decreased Inferred relationship Some 3
Arthrofibrosis Has interpretation True Decreased Inferred relationship Some 2
Arthrofibrosis of joint of left wrist region Has interpretation True Decreased Inferred relationship Some 2
Arthrofibrosis of right elbow Has interpretation True Decreased Inferred relationship Some 2
Arthrofibrosis of left shoulder (disorder) Has interpretation True Decreased Inferred relationship Some 2
Arthrofibrosis of left knee (disorder) Has interpretation True Decreased Inferred relationship Some 2
Arthrofibrosis of joint of left ankle region (disorder) Has interpretation True Decreased Inferred relationship Some 2
Arthrofibrosis of joint of finger of left hand Has interpretation True Decreased Inferred relationship Some 2
Arthrofibrosis of left elbow Has interpretation True Decreased Inferred relationship Some 2
Arthrofibrosis of right knee (disorder) Has interpretation True Decreased Inferred relationship Some 2
Arthrofibrosis of joint of right wrist region Has interpretation True Decreased Inferred relationship Some 2
Arthrofibrosis of joint of bilateral wrist regions (disorder) Has interpretation True Decreased Inferred relationship Some 3
Arthrofibrosis of joint of left hand (disorder) Has interpretation True Decreased Inferred relationship Some 2
Arthrofibrosis of joint of right hand Has interpretation True Decreased Inferred relationship Some 2
Arthrofibrosis of joint of finger of right hand Has interpretation True Decreased Inferred relationship Some 2
Arthrofibrosis of right shoulder Has interpretation True Decreased Inferred relationship Some 2
Bilateral arthrofibrosis fibrosis of knees Has interpretation True Decreased Inferred relationship Some 3
Arthrofibrosis of joint of bilateral ankle regions (disorder) Has interpretation True Decreased Inferred relationship Some 3
Arthrofibrosis of joint of right ankle region Has interpretation True Decreased Inferred relationship Some 2
Arthrofibrosis of joint of bilateral hands (disorder) Has interpretation True Decreased Inferred relationship Some 3
Arthrofibrosis of joint of ankle Has interpretation True Decreased Inferred relationship Some 2
Arthrofibrosis of joint of hand Has interpretation True Decreased Inferred relationship Some 2
Arthrofibrosis of joint of wrist region Has interpretation True Decreased Inferred relationship Some 2
Arthrofibrosis of joint of elbow Has interpretation True Decreased Inferred relationship Some 2
Arthrofibrosis of joint of knee Has interpretation True Decreased Inferred relationship Some 2
Arthrofibrosis of joint of shoulder region Has interpretation True Decreased Inferred relationship Some 2
Otodental syndrome (disorder) Has interpretation True Decreased Inferred relationship Some 2
46,XX ovarian dysgenesis, short stature syndrome (disorder) Has interpretation True Decreased Inferred relationship Some 2
Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome (disorder) Has interpretation True Decreased Inferred relationship Some 1
Albinism with deafness syndrome (disorder) Has interpretation True Decreased Inferred relationship Some 3
Myosin binding protein C1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome (disorder) Has interpretation True Decreased Inferred relationship Some 4
Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome (disorder) Has interpretation True Decreased Inferred relationship Some 4
Intellectual disability, macrocephaly, hypotonia, behavioural abnormalities syndrome Has interpretation True Decreased Inferred relationship Some 4
Waardenburg syndrome type 3 (disorder) Has interpretation True Decreased Inferred relationship Some 4
Waardenburg syndrome Has interpretation True Decreased Inferred relationship Some 3
Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease (disorder) Has interpretation True Decreased Inferred relationship Some 4
Waardenburg Shah syndrome Has interpretation True Decreased Inferred relationship Some 6
Waardenburg syndrome type 2 (disorder) Has interpretation True Decreased Inferred relationship Some 3
Waardenburg syndrome type 1 (disorder) Has interpretation True Decreased Inferred relationship Some 3
Myopathic Ehlers-Danlos syndrome (disorder) Has interpretation True Decreased Inferred relationship Some 6
Senter syndrome Has interpretation True Decreased Inferred relationship Some 4
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Has interpretation True Decreased Inferred relationship Some 5
Keratitis ichthyosis and deafness syndrome (disorder) Has interpretation True Decreased Inferred relationship Some 4
Hypothalamic adipsic hypernatremia syndrome (disorder) Has interpretation True Decreased Inferred relationship Some 1
Juvenile-onset diabetes mellitus, central and peripheral neurodegeneration syndrome (disorder) Has interpretation True Decreased Inferred relationship Some 3
Congenital contracture of limbs and face, hypotonia, developmental delay syndrome Has interpretation True Decreased Inferred relationship Some 3
Hypohidrosis due to neurological disorder (disorder) Has interpretation True Decreased Inferred relationship Some 1
Finding of decreased risk level (finding) Has interpretation True Decreased Inferred relationship Some 1
Antenatal multi-minicore disease with arthrogryposis multiplex congenita Has interpretation True Decreased Inferred relationship Some 3
Syndromic sensorineural deafness due to combined oxidative phosphorylation defect Has interpretation True Decreased Inferred relationship Some 2
Non-syndromic genetic hearing loss Has interpretation True Decreased Inferred relationship Some 1

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