900000000000490003: Description inactivation indicator attribute value reference set (foundation metadata concept)

SNOMED CT Concept\SNOMED CT Model Component\Foundation metadata concept (foundation metadata concept)\Reference set\Attribute value type\Description inactivation indicator reference set

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Description inactivation indicator reference set	Is a	Attribute value type	true	Inferred relationship	Some

Members	valueId
950	Concept non-current
950 (qualifier value)	Concept non-current
96	Concept non-current
96 (qualifier value)	Concept non-current
96.5	Concept non-current
96.5 (qualifier value)	Concept non-current
960	Concept non-current
960 (qualifier value)	Concept non-current
96000000	Concept non-current
96000000 (qualifier value)	Concept non-current
97	Concept non-current
97 (qualifier value)	Concept non-current
97.2	Concept non-current
97.2 (qualifier value)	Concept non-current
975	Concept non-current
975 (qualifier value)	Concept non-current
98	Concept non-current
98 (qualifier value)	Concept non-current
980	Concept non-current
980 (qualifier value)	Concept non-current
99	Concept non-current
99 (qualifier value)	Concept non-current
99.5	Concept non-current
99.5 (qualifier value)	Concept non-current
99.74	Concept non-current
99.74 (qualifier value)	Concept non-current
99.9	Concept non-current
99.9 (qualifier value)	Concept non-current
99.96	Concept non-current
99.96 (qualifier value)	Concept non-current
990	Concept non-current
990 (qualifier value)	Concept non-current
999	Concept non-current
999 (qualifier value)	Concept non-current
999.34	Concept non-current
999.34 (qualifier value)	Concept non-current
9am cortisol level	Concept non-current
9am cortisol level	Concept non-current
9am cortisol level (procedure)	Concept non-current
9am cortisol level (procedure)	Concept non-current
9p minus syndrome	Concept non-current
9p monosomy syndrome	Concept non-current
9p partial monosomy syndrome	Concept non-current
9p partial monosomy syndrome (disorder)	Concept non-current
9q22.3 deletion syndrome	Concept non-current
9q22.3 deletion syndrome (disorder)	Concept non-current
:: Gamma heavy chain disease	Concept non-current
<1.5 hours sent off: [DS4] or [DS1500]	Concept non-current
<1.5 hours sent off: [DS4] or [DS1500] (finding)	Concept non-current
<3	Concept non-current
<3 (qualifier value)	Concept non-current
<90	Concept non-current
<90 (qualifier value)	Concept non-current
>2.5 hours sent off: [DS4] or [DS1500]	Concept non-current
>2.5 hours sent off: [DS4] or [DS1500] (finding)	Concept non-current
>5	Concept non-current
>5 (qualifier value)	Concept non-current
>90	Concept non-current
>90 (qualifier value)	Concept non-current
>97	Concept non-current
>97 (qualifier value)	Concept non-current
? child now: [EC69] or [EC60] from FPC] or [EC69 from HB]	Concept non-current
? child now: [EC69] or [EC60] from FPC] or [EC69 from HB]	Concept non-current
? child now: [EC69] or [EC60] from FPC] or [EC69 from HB] (finding)	Concept non-current
? child now: [EC69] or [EC60] from FPC] or [EC69 from HB] (finding)	Concept non-current
? patient now: [FP69 from FPC] or [GP69 from HB]	Concept non-current
? patient now: [FP69 from FPC] or [GP69 from HB]	Concept non-current
? patient now: [FP69 from FPC] or [GP69 from HB] (finding)	Concept non-current
? patient now: [FP69 from FPC] or [GP69 from HB] (finding)	Concept non-current
A	Concept non-current
A & E doctor	Nonconformance to editorial policy component (foundation metadata concept)
A (tumor staging)	Concept non-current
A - alphalipoproteinaemia neuropathy	Nonconformance to editorial policy component (foundation metadata concept)
A - alphalipoproteinemia neuropathy	Nonconformance to editorial policy component (foundation metadata concept)
A 1 to 5 cm firm lesion raised above the surface of the surrounding skin; differs from a papule only in size	Erroneous component (foundation metadata concept)
A Noonan-related syndrome with characteristics of facial anomalies suggestive of Noonan syndrome, a distinctive hair anomaly described as loose anagen hair syndrome, frequent congenital heart defects, distinctive skin features with darkly pigmented skin, keratosis pilaris, eczema or occasional neonatal ichthyosis and short stature, often associated with a growth hormone deficiency and psychomotor delay. There is evidence that this syndrome is caused by heterozygous mutation in the SHOC2 gene on chromosome 10q25.	Outdated component (foundation metadata concept)
A Wernicke-like encephalopathy with characteristics of seizures responsive to high doses of thiamine. Two cases have been described so far. Clinical features include epilepsy, nystagmus, ophthalmoplegia and ataxia. The disease results from mutations in the SLC19A3 gene, encoding a thiamine transporter. Transmission is autosomal recessive.	Outdated component (foundation metadata concept)
A acquired demyelinating neuropathy disease with characteristics of acute symmetric monophasic sensory neuropathy without motor involvement, typically manifesting with numbness in the distal lower limbs which progressively extends to all the limb, tingling sensation in the distal lower limbs, generalised areflexia and unsteady gait as well as clumsiness of the upper limbs, pseudoathetosis and loss of vibration sense.	Outdated component (foundation metadata concept)
A acquired demyelinating neuropathy disease with characteristics of acute symmetric monophasic sensory neuropathy without motor involvement, typically manifesting with numbness in the distal lower limbs which progressively extends to all the limb, tingling sensation in the distal lower limbs, generalized areflexia and unsteady gait as well as clumsiness of the upper limbs, pseudoathetosis and loss of vibration sense.	Outdated component (foundation metadata concept)
A basal ganglia disorder with manifestation of parkinsonian-type symptoms (postural changes, tremor, rigidity), megalencephaly and variable intellectual deficit. Other signs are frontal bossing, persistent frontal lobe reflexes, strabismus and seizures. It has been described in three generations of one family. Transmission is X-linked, and the gene is located on chromosomal region Xq27.3-qter.	Outdated component (foundation metadata concept)
A basal subtype of epidermolysis bullosa simplex characterised by generalised blistering associated with muscular dystrophy. Onset of blistering is usually as early as birth, muscular dystrophy manifests between infancy and adulthood. Blisters are often haemorrhagic and heal with mild atrophic scarring and rare milia formation. Associated findings comprise markedly dystrophic nails, and focal keratoderma of the palms and soles. Extracutaneous involvement is usually present. Caused by mutations in the PLEC gene (8q24) encoding plectin. Plectin deficiency can be demonstrated in skin and muscle by analysis with specific antibodies. Transmission is autosomal recessive.	Outdated component (foundation metadata concept)
A basal subtype of epidermolysis bullosa simplex characterised by generalised or, less frequently, localised acral blistering. 19 cases have been reported to date. Onset of the disease is usually at birth. Milia are rare but atrophic scarring and dystrophic nails usually occur, along with focal keratoderma (palms and soles) and rarely ichthyotic plaques. Extracutaneous involvement is common, including anaemia, growth retardation, oral cavity abnormalities (blisters and erosions, and caries) and constipation. Due to mutations in the KRT14 gene (17q12-q21), encoding keratin 14. Transmission is autosomal recessive.	Outdated component (foundation metadata concept)
A basal subtype of epidermolysis bullosa simplex characterised by generalised severe blistering with widespread congenital absence of skin and pyloric atresia. Prevalence is unknown, but at least 12 families have been reported to date. Onset is at birth and babies are usually born prematurely with a low weight and poor general condition. Most cases are due to mutations in the PLEC gene (8q24) encoding the plectin 1 protein. Transmission is autosomal recessive.	Outdated component (foundation metadata concept)
A basal subtype of epidermolysis bullosa simplex characterized by generalized blistering associated with muscular dystrophy. Onset of blistering is usually as early as birth, muscular dystrophy manifests between infancy and adulthood. Blisters are often hemorrhagic and heal with mild atrophic scarring and rare milia formation. Associated findings comprise markedly dystrophic nails, and focal keratoderma of the palms and soles. Extracutaneous involvement is usually present. Caused by mutations in the PLEC gene (8q24) encoding plectin. Plectin deficiency can be demonstrated in skin and muscle by analysis with specific antibodies. Transmission is autosomal recessive.	Outdated component (foundation metadata concept)
A basal subtype of epidermolysis bullosa simplex characterized by generalized or, less frequently, localized acral blistering. 19 cases have been reported to date. Onset of the disease is usually at birth. Milia are rare but atrophic scarring and dystrophic nails usually occur, along with focal keratoderma (palms and soles) and rarely ichthyotic plaques. Extracutaneous involvement is common, including anemia, growth retardation, oral cavity abnormalities (blisters and erosions, and caries) and constipation. Due to mutations in the KRT14 gene (17q12-q21), encoding keratin 14. Transmission is autosomal recessive.	Outdated component (foundation metadata concept)
A basal subtype of epidermolysis bullosa simplex characterized by generalized severe blistering with widespread congenital absence of skin and pyloric atresia. Prevalence is unknown, but at least 12 families have been reported to date. Onset is at birth and babies are usually born prematurely with a low weight and poor general condition. Most cases are due to mutations in the PLEC gene (8q24) encoding the plectin 1 protein. Transmission is autosomal recessive.	Outdated component (foundation metadata concept)
A basal subtype of epidermolysis bullosa simplex with manifestation of belt-like areas of erythema with multiple vesicles and small blisters at the advancing edge of erythema. Prevalence is unknown but 2 families have been reported to date. Onset of the disease is usually at birth. The lesions occur on the limbs and trunk and heal with brown pigmentation but no scarring. Extracutaneous involvement is absent. The disease is due to a specific mutation in the KRT5 (12q13.13) gene, encoding keratin 5. Transmission is autosomal dominant.	Outdated component (foundation metadata concept)
A benign autosomal dominant form of slowly progressive muscular dystrophy. To date, fewer than 100 cases have been reported in the literature, thus illustrating its rarity. The clinical features do not differ markedly from those of other mild forms of progressive muscular dystrophy with the exception of finger contractures that are sometimes suggestive of the diagnosis. Creatine kinase levels and histological findings are not conclusive. Mutations in one of the three subunits of collagen VI are responsible for the disease. Molecular studies are however hampered by the size and expression pattern of the genes. Treatment remains purely supportive.	Outdated component (foundation metadata concept)
A benign form of holoprosencephaly with characteristics of midline defects without the typical holoprosencephaly defect in brain cleavage and which can variably manifest with microcephaly, hypotelorism, midline cleft lip and/or flat nose, choanal stenosis, pyriform sinus stenosis, coloboma as well as a single median maxillary incisor.	Outdated component (foundation metadata concept)
A benign genetic condition with characteristic of persistence of high alpha-fetoprotein (AFP) levels throughout life, with no associated clinical disability and thus no need for specific therapy.	Outdated component (foundation metadata concept)
A benign natural killer (NK) cell lymphoproliferative disease with characteristics of minor abdominal symptoms (abdominal pain, diverticulosis, constipation and reflux) due to NK cell-derived lesions in the mucosal layer of the gastrointestinal tract and often mistaken for NK or T-cell lymphoma.	Outdated component (foundation metadata concept)
A benign or malignant neoplasm arising primarily in the inner lining, muscle layer, or the surrounding pericardium of the heart. They can be primary or metastatic. Primary cardiac neoplasms are rare in children. The vast majority of primary cardiac neoplasms in children are benign, whilst approximately 10% are malignant. In contrast, the majority of secondary neoplasms are malignant.	Outdated component (foundation metadata concept)
A bleeding disorder with characteristics of mild to moderate mucocutaneous bleeding, which becomes more pronounced during pregnancy or following ingestion of drugs that have anti-platelet activity. This disease is due to hyperresponsive platelets, resulting in thrombocytopenia.	Outdated component (foundation metadata concept)
A body cavity route that begins within the peritoneal cavity and that has the propensity for absorption via the peritoneal membrane.	Nonconformance to editorial policy component (foundation metadata concept)
A bone dysplasia with manifestation of bone fragility, frequent bone fractures at a young age, cemento-osseous lesions of the jaw bones, bowing of tubular bones (tibia and fibula) and diaphyseal sclerosis of long bones. Autosomal dominant mode of transmission.	Outdated component (foundation metadata concept)
A brain malformation due to abnormal neuronal migration, in which a subset of neurons fails to migrate into the developing cerebral cortex and remains as nodules that line the ventricular surface. Classical periventricular nodular heterotopia is a rare X-linked dominant disorder far more frequent in females who present normal intelligence to borderline intellectual deficit, epilepsy of variable severity and extra-central nervous system signs, especially cardiovascular defects or coagulopathy. The disorder is generally associated with prenatal lethality in males.	Outdated component (foundation metadata concept)
A branchial arch syndrome with characteristics of supernumerary nipples, preauricular appendages and often binocular epibulbar lipodermoids or unilateral subconjunctival lipodermoids.	Outdated component (foundation metadata concept)
A cauterisation done with thermal energy.	Nonconformance to editorial policy component (foundation metadata concept)
A cauterization done with thermal energy	Erroneous component (foundation metadata concept)
A cauterization done with thermal energy.	Nonconformance to editorial policy component (foundation metadata concept)
A central nervous system malformation syndrome with characteristics of holoprosencephaly with microcephaly, abnormal eye morphology (hypotelorism, cyclopia, exophthalmos), nasal anomalies (single nostril or absent nose), and cleft lip/palate, combined with signs of caudal regression (sacral agenesis, sirenomelia with absent external genitalia).	Outdated component (foundation metadata concept)

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Reference Sets

Reference set descriptor

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Id	Description	Lang	Type	Status	Case?	Module
900000000001069012	Description inactivation indicator attribute value reference set	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)
900000000001070013	Description inactivation indicator reference set	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)
900000000001071012	Description inactivation indicator attribute value reference set (foundation metadata concept)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)