1250004: Decreased (qualifier value)

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

\Finding status values\Change values\Changed status\Decreased

\Degree findings\Decreased

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
Decreased	Is a	Degree findings	true	Inferred relationship	Some
Decreased	Is a	General adjectival modifier	false	Inferred relationship	Some
Decreased	Is a	Changed status	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Failed attempted abortion with oliguria (disorder)	Has interpretation	True	Decreased	Inferred relationship	Some	1
Legal abortion with oliguria	Has interpretation	False	Decreased	Inferred relationship	Some	1
Miscarriage with oliguria (disorder)	Has interpretation	True	Decreased	Inferred relationship	Some	1
Oliguria (finding)	Has interpretation	True	Decreased	Inferred relationship	Some	1
oligurie compliquant une intervention	Has interpretation	False	Decreased	Inferred relationship	Some	1
Deficient urine secretion	Has interpretation	True	Decreased	Inferred relationship	Some	1
Suppressed urine secretion	Has interpretation	True	Decreased	Inferred relationship	Some	1
Induced termination of pregnancy complicated by acute renal failure with oliguria (disorder)	Has interpretation	True	Decreased	Inferred relationship	Some	1
Induced termination of pregnancy complicated by oliguria	Has interpretation	True	Decreased	Inferred relationship	Some	1
Decline in functional status (finding)	Has interpretation	True	Decreased	Inferred relationship	Some	1
Decreased mobility of tympanic membrane (finding)	Has interpretation	True	Decreased	Inferred relationship	Some	2
Syncope due to autonomic failure	Has interpretation	True	Decreased	Inferred relationship	Some	5
Trunk feels cold	Has interpretation	True	Decreased	Inferred relationship	Some	1
Cardiac stroke volume index is the the volume of blood ejected per beat divided by body surface area, hence units of measurement are ml/m square - (cardiac) stroke volume index is therefore a more precise individual measurement.	Has interpretation	True	Decreased	Inferred relationship	Some	2
Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (disorder)	Has interpretation	True	Decreased	Inferred relationship	Some	1
A rare heterogeneous group of metabolic disorders characterized by abnormal calcium metabolism causing hypocalcemia due to insufficient serum levels of bioactive parathormone (PTH), without other endocrine disorders or developmental defects.	Has interpretation	True	Decreased	Inferred relationship	Some	4
Decreased withdrawn behavior (finding)	Has interpretation	False	Decreased	Inferred relationship	Some	2
Decreased social isolation (finding)	Has interpretation	False	Decreased	Inferred relationship	Some	1
Decreased despair (finding)	Has interpretation	True	Decreased	Inferred relationship	Some	1
Hereditary isolated hypoparathyroidism due to agenesis of parathyroid gland (disorder)	Has interpretation	True	Decreased	Inferred relationship	Some	1
Decreased or absent display of maxillary and/or the mandibular incisal edge at rest.	Has interpretation	True	Decreased	Inferred relationship	Some	1
Decreased display of the maxillary incisal during a posed smile. Normal display should involve the whole maxillary incisors and interdental gingiva.	Has interpretation	True	Decreased	Inferred relationship	Some	1
Congenital conductive hearing loss	Has interpretation	True	Decreased	Inferred relationship	Some	4
Benign granulocytopenia in childhood	Has interpretation	False	Decreased	Inferred relationship	Some	1
Chronic benign granulocytopenia	Has interpretation	False	Decreased	Inferred relationship	Some	1
Granulocytopenic disorder (disorder)	Has interpretation	False	Decreased	Inferred relationship	Some	1
Febrile granulocytopenia (disorder)	Has interpretation	False	Decreased	Inferred relationship	Some	1
Megaloblastic anaemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness	Has interpretation	True	Decreased	Inferred relationship	Some	3
Deficiency of testosterone biosynthesis	Has interpretation	True	Decreased	Inferred relationship	Some	1
Hypothyroidism following radioiodine therapy	Has interpretation	True	Decreased	Inferred relationship	Some	1
Iatrogenic ovarian failure	Has interpretation	True	Decreased	Inferred relationship	Some	1
Ovarian failure following radiotherapy	Has interpretation	True	Decreased	Inferred relationship	Some	2
Primary ovarian failure	Has interpretation	True	Decreased	Inferred relationship	Some	1
Iatrogenic testicular hypofunction	Has interpretation	True	Decreased	Inferred relationship	Some	1
Resistant ovary syndrome	Has interpretation	True	Decreased	Inferred relationship	Some	1
Leydig cell failure in adult	Has interpretation	True	Decreased	Inferred relationship	Some	1
Pure gonadal dysgenesis 46,XX	Has interpretation	True	Decreased	Inferred relationship	Some	1
Ovarian failure	Has interpretation	True	Decreased	Inferred relationship	Some	1
Testicular hypofunction	Has interpretation	True	Decreased	Inferred relationship	Some	1
Hypothyroidism caused by radiation	Has interpretation	True	Decreased	Inferred relationship	Some	1
Postablative ovarian failure	Has interpretation	True	Decreased	Inferred relationship	Some	1
Postablative testicular hypofunction	Has interpretation	True	Decreased	Inferred relationship	Some	1
Ovarian dysgenesis	Has interpretation	True	Decreased	Inferred relationship	Some	1
Post-chemotherapy testicular hypofunction	Has interpretation	True	Decreased	Inferred relationship	Some	1
Menopause ovarian failure	Has interpretation	False	Decreased	Inferred relationship	Some	1
Postablative hypothyroidism	Has interpretation	True	Decreased	Inferred relationship	Some	1
Post-chemotherapy ovarian failure	Has interpretation	True	Decreased	Inferred relationship	Some	1
Premature ovarian failure (disorder)	Has interpretation	True	Decreased	Inferred relationship	Some	1
Autoimmune primary ovarian failure	Has interpretation	True	Decreased	Inferred relationship	Some	1
Secondary ovarian failure	Has interpretation	True	Decreased	Inferred relationship	Some	1
Testicular hypofunction due to defect in adrenocortical hormone synthesis	Has interpretation	True	Decreased	Inferred relationship	Some	1
Primary testicular failure (disorder)	Has interpretation	True	Decreased	Inferred relationship	Some	1
Iatrogenic premature ovarian failure (disorder)	Has interpretation	True	Decreased	Inferred relationship	Some	1
Acquired premature ovarian failure	Has interpretation	False	Decreased	Inferred relationship	Some	1
Idiopathic premature ovarian failure (disorder)	Has interpretation	True	Decreased	Inferred relationship	Some	1
Premature ovarian failure due to autoimmune oophoritis (disorder)	Has interpretation	True	Decreased	Inferred relationship	Some	1
Testicular hypofunction following procedure (disorder)	Has interpretation	True	Decreased	Inferred relationship	Some	1
Lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome is characterized by immune deficiency, gonadal dysgenesis and fatal lung fibrosis. So far, it has been described in two sisters born to consanguineous parents. Both karyotypes were normal female (46,XX). No genetic anomalies could be identified by comparative genome hybridization analysis of their genomes or by analysis of genes known to be associated with these types of anomalies.	Has interpretation	True	Decreased	Inferred relationship	Some	1
A rare genetic disease characterized by sclerosing dysplasia affecting the diaphyseal and metaphyseal regions of the long bones, as well as the skull and metacarpals, in association with skin changes like those seen in ichthyosis vulgaris and premature ovarian failure with bilateral hypoplasia of the ovaries. Patients present in adulthood, primarily with swelling of the extremities and occasional mild pain in the legs.	Has interpretation	True	Decreased	Inferred relationship	Some	2
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus.	Has interpretation	True	Decreased	Inferred relationship	Some	2
Ovarian failure due to procedure (disorder)	Has interpretation	True	Decreased	Inferred relationship	Some	1
Symptomatic postprocedural ovarian failure	Has interpretation	False	Decreased	Inferred relationship	Some	1
insuffisance testiculaire postradique	Has interpretation	False	Decreased	Inferred relationship	Some	2
Incomplete loss of consciousness without amnesia (finding)	Has interpretation	True	Decreased	Inferred relationship	Some	1
Cytotoxic drug-induced hypospermatogenesis	Has interpretation	True	Decreased	Inferred relationship	Some	2
Hypospermatogenesis (finding)	Has interpretation	True	Decreased	Inferred relationship	Some	2
Hypothyroidism following external radiotherapy (disorder)	Has interpretation	True	Decreased	Inferred relationship	Some	2
Constrictive pericarditis	Has interpretation	True	Decreased	Inferred relationship	Some	3
Dysmorphism-conductive hearing loss-heart defect syndrome is a rare, multiple congenital anomalies syndrome characterized by a distinctive facial appearance (low frontal hairline, bilateral ptosis, prominent eyes, flat midface, broad, flat nares, Cupid bow upper lip vermilion, and small, low-set, posteriorly rotated ears), in addition to cleft palate, conductive hearing loss, heart defects (atrial or ventricular septal defect) and mild developmental delay/intellectual disability.	Has interpretation	True	Decreased	Inferred relationship	Some	2
Congenital trigeminal anesthesia is a rare neuro-ophthalmological disorder characterized by a congenital sensory deficit involving all or some of the sensory components of the trigeminal nerve. Due to corneal anesthesia, it usually presents with recurrent, painless eye infections, painless corneal opacities and/or poorly healing, ulcerated wounds on the facial skin and mucosa (typically the buccal mucosa and/or nasal septum).	Has interpretation	True	Decreased	Inferred relationship	Some	1
Decreased thickness of skin	Has interpretation	True	Decreased	Inferred relationship	Some	1
A rare genetic male infertility due to oligozoospermia (number of sperm in the ejaculate inferior to 15 million/mL) resulting from a mutation in a single gene known to cause oligozoospermia. Sperm morphology may be normal.	Has interpretation	True	Decreased	Inferred relationship	Some	1
Hypoparathyroidism	Has interpretation	True	Decreased	Inferred relationship	Some	1
Hypomagnesemia with secondary hypocalcemia (disorder)	Has interpretation	True	Decreased	Inferred relationship	Some	3
Transitory neonatal hypoparathyroidism	Has interpretation	True	Decreased	Inferred relationship	Some	1
Secondary hypoparathyroidism (disorder)	Has interpretation	True	Decreased	Inferred relationship	Some	1
Hypoparathyroidism after external beam radiotherapy (disorder)	Has interpretation	True	Decreased	Inferred relationship	Some	1
Hypoparathyroidism due to hemochromatosis (disorder)	Has interpretation	True	Decreased	Inferred relationship	Some	1
Idiopathic parathyroidism	Has interpretation	False	Decreased	Inferred relationship	Some	1
Hypoparathyroidism-sensorineural deafness-renal disease syndrome is a rare, clinically heterogeneous genetic disorder characterized by the triad of hypoparathyroidism (H), sensorineural deafness (D) and renal disease (R).	Has interpretation	True	Decreased	Inferred relationship	Some	5
Transient neonatal hypoparathyroidism due to maternal hyperparathyroidism (disorder)	Has interpretation	True	Decreased	Inferred relationship	Some	1
Transient hypoparathyroidism	Has interpretation	True	Decreased	Inferred relationship	Some	1
Neonatal hypoparathyroidism	Has interpretation	True	Decreased	Inferred relationship	Some	1
Idiopathic hypoparathyroidism	Has interpretation	True	Decreased	Inferred relationship	Some	1
Hypoparathyroidism due to granulomatous disease (disorder)	Has interpretation	True	Decreased	Inferred relationship	Some	1
X-linked hypoparathyroidism (disorder)	Has interpretation	True	Decreased	Inferred relationship	Some	1
Hypoparathyroidism - autosomal dominant	Has interpretation	False	Decreased	Inferred relationship	Some	1
A rare, genetic, disease that manifests in childhood or early adolescence with a combination of chronic mucocutaneous candidiasis, hypoparathyroidism and autoimmune adrenal failure.	Has interpretation	True	Decreased	Inferred relationship	Some	1
Kenny syndrome	Has interpretation	True	Decreased	Inferred relationship	Some	2
Hypoparathyroidism after iodine thyroid ablation (disorder)	Has interpretation	True	Decreased	Inferred relationship	Some	1
Hypoparathyroidism due to impaired PTH secretion	Has interpretation	True	Decreased	Inferred relationship	Some	1
Isolated late onset hypoparathyroidism	Has interpretation	True	Decreased	Inferred relationship	Some	1
Isolated persistent neonatal hypoparathyroidism	Has interpretation	True	Decreased	Inferred relationship	Some	1
Hypoparathyroidism following procedure (disorder)	Has interpretation	True	Decreased	Inferred relationship	Some	1
Postablative hypoparathyroidism	Has interpretation	True	Decreased	Inferred relationship	Some	2
Postablative hypoparathyroidism	Has interpretation	False	Decreased	Inferred relationship	Some	1
Post-surgical hypoparathyroidism	Has interpretation	True	Decreased	Inferred relationship	Some	1
Autoimmune hypoparathyroidism	Has interpretation	True	Decreased	Inferred relationship	Some	1
Parathyroid hypocalcemic tetany	Has interpretation	True	Decreased	Inferred relationship	Some	1
A rare multiple congenital anomalies/dysmorphic syndrome characterized by the association of congenital hypoparathyroidism, nephropathy, congenital lymphedema, mitral valve prolapse and brachytelephalangy. Additional features include mild facial dysmorphism, hypertrichosis, and nail abnormalities. There have been no further descriptions in the literature since 1993.	Has interpretation	True	Decreased	Inferred relationship	Some	3
Flat anterior chamber of eye with hypotony	Has interpretation	True	Decreased	Inferred relationship	Some	1

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Reference Sets

Description inactivation indicator reference set

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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