41847000: Adulthood (qualifier value)

SNOMED CT Concept\Qualifier value\...

\Precondition value (qualifier value)\Periods of life\Any period of life commencing after birth, but before death.\Adulthood

\Special atomic mapping values\Special disorder atoms\Temporal periods\Periods of life\Any period of life commencing after birth, but before death.\Adulthood

\Descriptor (qualifier value)\Time patterns\Temporal periods\Periods of life\Any period of life commencing after birth, but before death.\Adulthood

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
Adulthood	Is a	Age AND/OR growth period (observable entity)	false	Inferred relationship	Some
Adulthood	Is a	Periods of life	false	Inferred relationship	Some
Adulthood	Is a	Any period of life commencing after birth, but before death.	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Acquired angio-oedema due to the presence of neutralising antibodies against C1 inhibitor.	Occurrence	False	Adulthood	Inferred relationship	Some	1
A rare non-histaminic angioedema characterised by potentially life-threatening episodes of oedema of subcutaneous and/or mucosal tissues without urticaria, caused by excessive consumption of C1 esterase inhibitor (C1-INH) in the context of lymphoproliferative or autoimmune diseases. Patients typically present in the fourth decade of life or later and without a family history of angioedema. Clinical manifestation includes nonpitting oedema of the skin predominantly involving the face, but also the limbs or genitals, as well as abdominal pain due to involvement of the gastrointestinal mucosa and severe oedema of the upper airway and oral mucosa. Laboratory examination shows low C1-INH activity and low C3, C4, and C1q levels. Autoantibodies to C1-INH are frequently detectable.	Occurrence	False	Adulthood	Inferred relationship	Some	2
Adult Fanconi syndrome	Occurrence	True	Adulthood	Inferred relationship	Some	1
Erhvervet megacolon hos voksne	Occurrence	False	Adulthood	Inferred relationship	Some	1
Erhvervet megacolon hos voksne	Occurrence	False	Adulthood	Inferred relationship	Some	2
Epidermolysis bullosa acquisita, classical acral type (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Epidermolysis bullosa acquisita, bullous pemphigoid-like (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Epidermolysis bullosa acquisita, cicatricial pemphigoid-like (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Epidermolysis bullosa acquisita, Brunsting-Perry type (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Acquired epidermolysis bullosa	Occurrence	True	Adulthood	Inferred relationship	Some	1
Epidermolysis bullosa acquisita, oral mucosal involvement (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Drug-induced epidermolysis bullosa acquisita (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
A very rare non-syndromic autosomal recessive pyridoxine-refractory sideroblastic anemia due to a splice defect of glutaredoxin-5 (GLRX5) described in a single patient with adult onset microcytic hypochromic anemia with liver iron overload and type 2 diabetes.	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult hydrocele	Occurrence	True	Adulthood	Inferred relationship	Some	1
A rare, genetic, non-dystrophic myofibrillar myopathy disorder characterized by late-adult onset of distal and/or proximal limb muscle weakness with initial involvement of posterior lower leg muscles, medial gastrocnemius and soleus. Patients present with ankle weakness followed by weakness of finger and wrist extensors and later on of proximal muscles. Ambulation is usually preserved. Late-onset associated cardiomyopathy and/or neuropathy has been reported in a minority of cases.	Occurrence	True	Adulthood	Inferred relationship	Some	1
Distal muscular dystrophy, Miyoshi type	Occurrence	True	Adulthood	Inferred relationship	Some	1
Distal myopathy with posterior leg and anterior hand involvement, also named distal ABD-filaminopathy, is a neuromuscular disease characterized by a progressive symmetric muscle weakness of anterior upper and posterior lower limbs.	Occurrence	True	Adulthood	Inferred relationship	Some	1
A rare, genetic distal myopathy disorder characterized by middle age-onset of distal leg muscle weakness, atrophy in the anterior compartment resulting in foot drop, without proximal or scapular skeletal muscle weakness. Rapidly progressive dementia, Paget disease of bone and hand weakness have been reported. Muscle biopsy shows pronounced myopathic changes with rimmed vacuoles.	Occurrence	True	Adulthood	Inferred relationship	Some	1
Distal myopathy with early respiratory muscle involvement	Occurrence	False	Adulthood	Inferred relationship	Some	1
Distal myopathy 2	Occurrence	True	Adulthood	Inferred relationship	Some	1
Tibial muscular dystrophy	Occurrence	True	Adulthood	Inferred relationship	Some	1
A rare distal myopathy characterized by weakness in the distal upper extremities, usually finger and wrist extensors which later progresses to all hand muscles and distal lower extremity, primarily in toe and ankle extensors.	Occurrence	True	Adulthood	Inferred relationship	Some	1
Finnish upper limb-onset distal myopathy is a rare, genetic distal myopathy characterized by slowly progressive distal to proximal limb muscle weakness and atrophy, with characteristic early involvement of thenar and hypothenar muscles. Patients present with clumsiness of the hands and stumbling in the fourth to fifth decade of life, and later develop steppage gait and contractures of the hands. Progressive fatty degeneration affects intrinsic muscles of the hands, gluteus medium and both anterior and posterior compartment muscles of the distal lower extremities, with later involvement of forearm muscles, triceps, infraspinatus and the proximal lower limb muscles. Asymmetry of muscle involvement is common.	Occurrence	True	Adulthood	Inferred relationship	Some	1
A rare genetic epidermal disease with characteristics of early childhood-onset of punctate palmoplantar keratoderma in association with adult-onset leukoencephalopathy manifested by progressive tetrapyramidal syndrome and cognitive deterioration.	Occurrence	False	Adulthood	Inferred relationship	Some	2
A rare autosomal recessive distal hereditary motor neuropathy with characteristics of slowly progressive muscular weakness, hypotonia and atrophy of the lower limbs, more pronounced distally, leading to paralysis, and loss of tendon reflexes. Additional features may include pes cavus and mild dysphonia. The upper limbs are relatively spared. There is evidence this disease is caused by homozygous mutation in the DNAJB2 gene on chromosome 2q35.	Occurrence	True	Adulthood	Inferred relationship	Some	1
Sexual abuse of adult (event)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Neglect of elder (event)	Occurrence	False	Adulthood	Inferred relationship	Some	1
Non-domestic physical abuse of adult (event)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Psychological abuse of adult	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult abuse (event)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult victim of abuse (finding)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Physical abuse of elderly person	Occurrence	False	Adulthood	Inferred relationship	Some	1
Emotional abuse of elderly person	Occurrence	False	Adulthood	Inferred relationship	Some	1
Deprivation of nourishment of elderly person	Occurrence	False	Adulthood	Inferred relationship	Some	1
Abandonment of elderly person	Occurrence	False	Adulthood	Inferred relationship	Some	1
Emotional abuse of adult	Occurrence	True	Adulthood	Inferred relationship	Some	1
Elderly person maltreatment	Occurrence	False	Adulthood	Inferred relationship	Some	1
Domestic sexual abuse of adult (event)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Physical abuse of adult	Occurrence	True	Adulthood	Inferred relationship	Some	1
Domestic abuse of adult	Occurrence	True	Adulthood	Inferred relationship	Some	1
Victim of elder abuse	Occurrence	False	Adulthood	Inferred relationship	Some	1
Psychologically abused elder	Occurrence	False	Adulthood	Inferred relationship	Some	2
A rare progressive muscular dystrophy characterized by an adult-onset scapulo-axio-peroneal myopathy. Clinical presentation includes shoulder girdle atrophy, scapular winging, axial muscular atrophy of postural muscles combined with a generalized hypertrophy. Typically neck rigidity, rigid spine, Achilles tendon shortening and respiratory insufficiency later in disease course are present. The phenotype is caused by mutation in the FHL1 gene.	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult atopic dermatitis recurrent in adult life (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
A rare genetic axonal hereditary motor and sensory neuropathy disorder with characteristics of adulthood-onset of slowly progressive, occasionally asymmetrical, distal muscle weakness and atrophy (predominantly in the lower limbs), pan-modal sensory loss, muscle cramping in extremities and/or trunk, pes cavus and absent or reduced deep tendon reflexes. Gait anomalies and variable autonomic disturbances, such as erectile dysfunction and urinary urgency, may be associated. The disease can be caused by homozygous or heterozygous mutation in the LRSAM1 gene on chromosome 9q33.	Occurrence	True	Adulthood	Inferred relationship	Some	2
A rare genetic axonal hereditary motor and sensory neuropathy disorder with characteristics of adulthood-onset of slowly progressive, occasionally asymmetrical, distal muscle weakness and atrophy (predominantly in the lower limbs), pan-modal sensory loss, muscle cramping in extremities and/or trunk, pes cavus and absent or reduced deep tendon reflexes. Gait anomalies and variable autonomic disturbances, such as erectile dysfunction and urinary urgency, may be associated. The disease can be caused by homozygous or heterozygous mutation in the LRSAM1 gene on chromosome 9q33.	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult onset Still's disease	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult onset autosomal recessive muscular dystrophy with normal dystrophin	Occurrence	True	Adulthood	Inferred relationship	Some	1
A rare genetic motor neuron disease with characteristics of slowly progressive predominantly proximal muscular weakness and atrophy which typically manifests with muscle cramps, fasciculations, decreased/absent deep tendon reflexes, hand tremor and elevated serum creatine kinase at onset and later associates gait disturbances and impaired vibration sensation. There is evidence the disease is caused by heterozygous mutation in the CHCHD10 gene on chromosome 22q11.	Occurrence	True	Adulthood	Inferred relationship	Some	1
A rare genetic disease with characteristics of adult-onset myofibrillar myopathy variably associated with cardiomyopathy and/or posterior pole cataracts. Patients typically present progressive proximal and distal muscle weakness and wasting of lower and upper limbs, often with velopharyngeal involvement including dysphagia, dysphonia and ventilatory insufficiency. Electromyography shows myopathic features and muscle biopsy reveals myofibrillar myopathy changes. Caused by heterozygous mutation in the alpha-B-crystallin gene (CRYAB) on chromosome 11q23.	Occurrence	True	Adulthood	Inferred relationship	Some	1
A rare genetic motor neuron disease with characteristics of adult-onset of slowly progressive proximal muscular weakness with fasciculations, amyotrophy, cramps and absent/hypoactive reflexes without bulbar or pyramidal involvement. Caused by heterozygous mutation in the gene encoding vesicle-associated membrane protein-associated protein B (VAPB) on chromosome 20q13.	Occurrence	True	Adulthood	Inferred relationship	Some	1
A rare acquired immunodeficiency disorder characterised by the appearance of susceptibility to disseminated opportunistic infections (in particular, disseminated nontuberculous mycobacterial infection, salmonellosis, penicillosis, and varicella zoster virus infection) in previously healthy (HIV-negative) adults, associated with the presence of acquired autoantibodies to interferon gamma. Typical clinical manifestation includes lymphadenopathy (cervical or generalised), fever, weight loss and/or reactive skin lesions.	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult atopic dermatitis persistent from childhood (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	2
Adult atopic dermatitis commencing in adult life (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	2
A rare genetic autosomal recessive cerebellar ataxia disease with characteristics of adulthood-onset of slowly progressive spinocerebellar ataxia, manifesting with gait and appendicular ataxia, dysarthria, ocular movement anomalies (for example horizontal, vertical, and/or downbeat nystagmus, hypermetric saccades), increased deep tendon reflexes and progressive cognitive decline. Additional variable features may include proximal leg muscle wasting and fasciculations, pes cavus, inspiratory stridor, epilepsy, retinal degeneration and cataracts. Brain imaging reveals marked cerebellar atrophy and electromyography shows evidence of lower motor neuron involvement. Caused by homozygous or compound heterozygous mutation in the ANO10 gene on chromosome 3p22.	Occurrence	True	Adulthood	Inferred relationship	Some	1
A rare genetic autosomal recessive cerebellar ataxia disease with characteristics of adulthood-onset of slowly progressive spinocerebellar ataxia, manifesting with gait and appendicular ataxia, dysarthria, ocular movement anomalies (for example horizontal, vertical, and/or downbeat nystagmus, hypermetric saccades), increased deep tendon reflexes and progressive cognitive decline. Additional variable features may include proximal leg muscle wasting and fasciculations, pes cavus, inspiratory stridor, epilepsy, retinal degeneration and cataracts. Brain imaging reveals marked cerebellar atrophy and electromyography shows evidence of lower motor neuron involvement. Caused by homozygous or compound heterozygous mutation in the ANO10 gene on chromosome 3p22.	Occurrence	True	Adulthood	Inferred relationship	Some	2
Adult osteochondritis of spine	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult osteochondritis of spine	Occurrence	True	Adulthood	Inferred relationship	Some	2
Adult bronchiectasis	Occurrence	True	Adulthood	Inferred relationship	Some	1
Malignant optic glioma of adulthood	Occurrence	True	Adulthood	Inferred relationship	Some	1
Cutaneous mastocytosis, adult form (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
generaliseret adult parodontit	Occurrence	False	Adulthood	Inferred relationship	Some	1
Voksen parodontit	Occurrence	False	Adulthood	Inferred relationship	Some	1
Lokal adult parodontit	Occurrence	False	Adulthood	Inferred relationship	Some	1
Epidermolysis bullosa acquisita, classical acral type (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	2
Epidermolysis bullosa acquisita, bullous pemphigoid-like (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	2
Epidermolysis bullosa acquisita, cicatricial pemphigoid-like (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	2
Epidermolysis bullosa acquisita, Brunsting-Perry type (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	2
Acquired epidermolysis bullosa	Occurrence	True	Adulthood	Inferred relationship	Some	2
Epidermolysis bullosa acquisita, oral mucosal involvement (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	2
Drug-induced epidermolysis bullosa acquisita (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	2
Adult atopic dermatitis (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	3
A rare acquired immunodeficiency disease with characteristics of adult-onset absolute neutrophil counts less than 1.5 x 10^9/L on at least 3 occasions in a 3 month period that cannot be attributable to drugs or a specific genetic, infectious, inflammatory, autoimmune or malignant cause. Recurrent apthous stomatitis and a history of mild bacterial infections are typically associated. A benign outcome with a low rate of severe infections and no secondary malignancies is observed.	Occurrence	True	Adulthood	Inferred relationship	Some	2
Adult onset fluency disorder	Occurrence	True	Adulthood	Inferred relationship	Some	2
Type IV adult Pelizaeus-Merzbacher disease	Occurrence	True	Adulthood	Inferred relationship	Some	1
Type IV adult Pelizaeus-Merzbacher disease	Occurrence	True	Adulthood	Inferred relationship	Some	2
A rare genetic macular dystrophy with characteristics of blurred vision, metamorphopsia and mild visual impairment secondary to a slightly elevated yellow egg yolk-like lesion located in the foveal or parafoveal region. Clinical onset is typically between the fourth and sixth decade of life. The mechanism underlying the physiopathology is unknown. An autosomal dominant inheritance with variable expression and incomplete penetrance is suggested but the disease can also be sporadic without evidence of a familial inheritance pattern.	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult linear immunoglobulin A disease	Occurrence	True	Adulthood	Inferred relationship	Some	1
Metachromatic leukodystrophy, adult type	Occurrence	True	Adulthood	Inferred relationship	Some	2
Metachromatic leukodystrophy, adult type	Occurrence	True	Adulthood	Inferred relationship	Some	1
Globoid cell leukodystrophy, late-onset	Occurrence	True	Adulthood	Inferred relationship	Some	1
Globoid cell leukodystrophy, late-onset	Occurrence	True	Adulthood	Inferred relationship	Some	2
Inclusion conjunctivitis of the adult	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult onset autosomal dominant leukodystrophy (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	2
Adult onset autosomal dominant leukodystrophy (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult retinoschisis (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult form of celiac disease	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult hypertrophic pyloric stenosis	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult acute epiglottitis and supraglottitis	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult onset dermatomyositis (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult onset dermatomyositis (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	2
Adult myxedema	Occurrence	True	Adulthood	Inferred relationship	Some	1
Hepatitis A virus antigen only adult vaccine product	This attribute represents a characteristic that is applicable to a product.	False	Adulthood	Inferred relationship	Some
Adult vaccine product containing only acellular Bordetella pertussis and Clostridium tetani toxoid and Corynebacterium diphtheriae toxoid antigens (medicinal product)	This attribute represents a characteristic that is applicable to a product.	False	Adulthood	Inferred relationship	Some
Adult vaccine product containing only Clostridium tetani and Corynebacterium diphtheriae toxoids (medicinal product)	This attribute represents a characteristic that is applicable to a product.	False	Adulthood	Inferred relationship	Some
A rare form of pterygium, which develops in early adulthood, characterised by a wing-like bulbar thickening of the conjunctiva in the interpalpebral fissure area that can be cured by surgical excision.	Occurrence	True	Adulthood	Inferred relationship	Some	1
A rare form of pterygium, which develops in early adulthood, characterised by a wing-like bulbar thickening of the conjunctiva in the interpalpebral fissure area that can be cured by surgical excision.	Occurrence	True	Adulthood	Inferred relationship	Some	2
Adult premenstrual acne	Occurrence	True	Adulthood	Inferred relationship	Some	1
Old age	Is a	True	Adulthood	Inferred relationship	Some
Middle age (qualifier value)	Is a	True	Adulthood	Inferred relationship	Some
Adult lichen sclerosus (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1

Start Page 2 of 3 End

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
69814016	Adulthood	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1203106017	Adulthood (qualifier value)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1229801011	Adulthood - period	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3970697015	Adult period of life	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1996571000005117	Voksenalder	da	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Danish module (core metadata concept)