41847000: Adulthood (qualifier value)

SNOMED CT Concept\Qualifier value (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	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
Adult lichen sclerosus (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Non-accidental injury to adult	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult T-cell leukaemia/lymphoma in remission	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult T-cell leukemia/lymphoma	Occurrence	True	Adulthood	Inferred relationship	Some	1
Multisystem inflammatory syndrome in adults	Occurrence	True	Adulthood	Inferred relationship	Some	1
Chronic idiopathic immunoneutropenia in adult (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	2
Pure autonomic failure (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	4
Multiple system atrophy	Occurrence	True	Adulthood	Inferred relationship	Some	1
Multiple system atrophy, cerebellar variant (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Multiple system atrophy, Parkinson variant (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Parkinsonian syndrome with idiopathic orthostatic hypotension (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	5
Adult osteomalacia due to liver disease	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult osteomalacia due to endocrine disease (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult behavior alteration (finding)	Occurrence	True	Adulthood	Inferred relationship	Some	2
Adult fucosidosis (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult infection of intestine caused by Clostridium botulinum	Occurrence	False	Adulthood	Inferred relationship	Some	2
Adult infection of intestine caused by Clostridium botulinum	Occurrence	False	Adulthood	Inferred relationship	Some	1
Domestic physical abuse of adult (event)	Occurrence	True	Adulthood	Inferred relationship	Some	1
A rare autosomal recessive limb-girdle muscular dystrophy characterized by adult onset of progressive muscle weakness and atrophy in the proximal upper and lower limbs, leading to scapular winging and loss of independent ambulation. Respiratory function may become impaired in the course of the disease. Fatty degeneration of internal regions of thigh muscles sparing external areas has been reported, as well as a reduction of alpha-dystroglycan in muscle biopsies.	Occurrence	True	Adulthood	Inferred relationship	Some	1
Ocular albinism with late-onset sensorineural deafness is a rare, X-linked inherited subtype of ocular albinism characterized by severe visual impairment, translucent pale-blue irises, a reduction in the retinal pigment and moderately severe deafness with onset ranging from adolescence to fourth or fifth decade of life.	Occurrence	True	Adulthood	Inferred relationship	Some	2
Adult osteomalacia due to malabsorption	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult osteomalacia due to malnutrition (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Nemaline myopathy, late onset type	Occurrence	True	Adulthood	Inferred relationship	Some	1
A rare carcinoma of the liver characterized by one to several or many nodules occurring anywhere within the liver, composed of neoplastic epithelial cells with hepatocellular differentiation. The vast majority of tumors are associated with chronic liver disease (such as hepatitis B or C, or steatohepatitis) or exposure to a variety of exogenous agents. Patients may present with signs and symptoms related to the tumor, as well as to the underlying condition. Common manifestations include right upper quadrant abdominal pain, weight loss, hepatosplenomegaly, jaundice, and ascites. Symptomatic tumors generally have poor prognosis.	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult osteochondrosis of thoracolumbar spine (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	2
Adult osteochondrosis of thoracic spine	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult osteochondrosis of cervical spine	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult osteochondrosis of thoracolumbar spine (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Primary lymphedema tardum (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Relapsing febrile nodular nonsuppurative panniculitis	Occurrence	True	Adulthood	Inferred relationship	Some	1
A rare bone disease characterized by spontaneous adult-onset tarsal navicular osteonecrosis. Patients present with chronic mid- and hindfoot pain, swelling and tenderness over the dorsomedial aspect of the midfoot, flattening of the medial longitudinal arch, and pes planovarus. Radiographic findings include comma-shaped deformity due to collapse of the lateral part of the navicular bone and medial or dorsal protrusion of a portion or the entire bone. The condition may be bilateral or asymmetric and associated with pathological fractures.	Occurrence	True	Adulthood	Inferred relationship	Some	1
A rare idiopathic inflammatory myopathy (IIM) with a heterogeneous phenotype characterized by myositis with at least one clinical and/or autoantibody overlap feature. Possible clinical overlap features include polyarthritis, Raynaud's phenomenon, sclerodactyly, scleroderma (proximal to metacarpophalangeal joints), lung interstitial pneumonia, and/or clinical signs of systemic lupus erythematosus (SLE).	Occurrence	True	Adulthood	Inferred relationship	Some	1
A rare biliary tract disease characterized by loss of interlobular bile ducts resulting in chronic cholestasis, without any known cause. Loss of less than 50% of interlobular bile ducts is associated with a mild disease course, while loss of the majority of ducts results in a severe form, potentially leading to cirrhosis and liver failure. Patients typically present as young or middle-aged adults with episodic jaundice, pruritus, and elevated liver enzymes.	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult chronic lichenified atopic dermatitis (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult chronic lichenified atopic dermatitis (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	2
Adult generalized atopic dermatitis (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult nummular atopic dermatitis (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult pruriginous atopic dermatitis (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult pruriginous atopic dermatitis (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	2
Adult impetiginized atopic dermatitis (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult atopic flexural dermatitis	Occurrence	True	Adulthood	Inferred relationship	Some	1
A rare progressive autosomal dominant macular dystrophy, presenting between the third and sixth decades of life, with characteristics of retinal atrophy and retinal detachment leading to loss of central vision, then peripheral vision, and eventually blindness.	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult pityriasis rubra pilaris	Occurrence	False	Adulthood	Inferred relationship	Some	3
Classical adult pityriasis rubra pilaris	Occurrence	False	Adulthood	Inferred relationship	Some	2
Atypical adult pityriasis rubra pilaris	Occurrence	False	Adulthood	Inferred relationship	Some	2
Adult degenerative scoliosis deformity of spine (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Amyotrophic lateral sclerosis with multiple system atrophy	Occurrence	True	Adulthood	Inferred relationship	Some	1
Alexander disease adult form	Occurrence	False	Adulthood	Inferred relationship	Some	1
Alexander disease adult form	Occurrence	False	Adulthood	Inferred relationship	Some	2
Adult-onset tic disorder (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult-onset sporadic primary dystonia	Occurrence	True	Adulthood	Inferred relationship	Some	1
Alexander disease adult form	Occurrence	False	Adulthood	Inferred relationship	Some	3
Primary malignant optic glioma of adulthood (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
A rare, genetic, macular dystrophy characterized by blurred vision, metamorphopsia and mild visual impairment secondary to a slightly elevated, yellow, egg yolk-like lesion located in the foveal or parafoveal region.	Occurrence	True	Adulthood	Inferred relationship	Some	2
Acquired megacolon in adult	Occurrence	True	Adulthood	Inferred relationship	Some	1
Idiopathic megacolon in adult	Occurrence	True	Adulthood	Inferred relationship	Some	1
Psychologically abused woman	Occurrence	True	Adulthood	Inferred relationship	Some	3
Psychological abuse complicating childbirth (finding)	Occurrence	True	Adulthood	Inferred relationship	Some	2
Psychological abuse complicating pregnancy (finding)	Occurrence	True	Adulthood	Inferred relationship	Some	4
A rare autosomal dominant limb-girdle muscular dystrophy characterized by adult onset of proximal muscle weakness, pain, and wasting predominantly affecting the proximal leg, lumbar paraspinal, and medial gastrocnemius muscles. Upper limb involvement may also be observed in some cases. Serum creatine kinase is often, but not always, elevated, and muscle biopsy shows non-specific myopathic changes. The severity of the disease is variable, although most patients remain ambulatory.	Occurrence	True	Adulthood	Inferred relationship	Some	1
Victim of human trafficking in adulthood (finding)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult intestinal botulism (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Infection of intestine caused by Clostridium botulinum in adulthood (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Sorsby pseudoinflammatory fundus dystrophy of left eye (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Sorsby pseudoinflammatory fundus dystrophy of right eye (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Sorsby pseudoinflammatory fundus dystrophy of bilateral eyes (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Sorsby pseudoinflammatory fundus dystrophy of bilateral eyes (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	2
A rare genetic neurological disorder characterised by congenital or early-onset sensorineural deafness and adult-onset progressive leucoencephalopathy. Progressive cognitive impairment and behavioural abnormalities are observed in the second or third decade of life, sometimes preceded by mild developmental delay and learning difficulties. Visual impairment in adult age has been reported. No central nervous system calcification is reported.	Occurrence	True	Adulthood	Inferred relationship	Some	3
Atypical adult pityriasis rubra pilaris	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult pityriasis rubra pilaris	Occurrence	True	Adulthood	Inferred relationship	Some	1
Classical adult pityriasis rubra pilaris	Occurrence	True	Adulthood	Inferred relationship	Some	1
Gender incongruence in adulthood	Occurrence	True	Adulthood	Inferred relationship	Some	1
Adult attention deficit hyperactivity disorder (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Intimate partner abuse	Occurrence	False	Adulthood	Inferred relationship	Some	1
A rare genetic systemic disease characterized by adult onset, progressive sensorimotor and autonomic neuropathy and infiltrative cardiomyopathy. Neurological involvement usually starts with sensory loss in the extremities and progresses with motor neuropathy. Cardiomyopathy presents with rhythm abnormalities and heart failure. The disease also frequently manifests with a range of additional clinical signs and symptoms due to associated ocular, renal, central nervous system and gastrointestinal involvement.	Occurrence	True	Adulthood	Inferred relationship	Some	1
A rare hereditary Transthyretin (TTR)-related systemic amyloidosis (ATTR) with predominant cardiac involvement resulting from myocardial infiltration of abnormal amyloid protein.	Occurrence	True	Adulthood	Inferred relationship	Some	1
Unexpected sudden death of adult	Occurrence	True	Adulthood	Inferred relationship	Some	1
Nutritional neglect of adult (event)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Neglect of adult (event)	Occurrence	True	Adulthood	Inferred relationship	Some	1
Neglected parents	Occurrence	True	Adulthood	Inferred relationship	Some	3
Adult-onset Steinert myotonic dystrophy (disorder)	Occurrence	True	Adulthood	Inferred relationship	Some	1

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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
360281000195115	età adulta	it	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
262101000077114	âge adulte	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
2371001000118	Erwachsenenalter	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module