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128293007: Chronic mental disorder (disorder)

Status: current, 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
206567015 Chronic mental illness en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
206568013 Chronic mental disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
206569017 Chronic mental disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
732269011 Chronic mental disorder (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
10401000188117 pathologie psychiatrique chronique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
73591000077115 maladie mentale chronique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
2414451000195111 Chronische psychische Krankheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
2414461000195114 Chronische psychische Störung de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

56 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Chronic mental disorder Is a Chronic disease true Inferred relationship Some
Chronic mental disorder Is a Mental disorder true Inferred relationship Some
Chronic mental disorder Course Chronic false Inferred relationship Some
Chronic mental disorder Clinical course Chronic true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Chronic alcoholic brain syndrome Is a False Chronic mental disorder Inferred relationship Some
toxicomanie chronique Is a False Chronic mental disorder Inferred relationship Some
Chronic major depressive disorder, single episode Is a True Chronic mental disorder Inferred relationship Some
Chronic recurrent major depressive disorder Is a False Chronic mental disorder Inferred relationship Some
Chronic bipolar I disorder, most recent episode depressed Is a True Chronic mental disorder Inferred relationship Some
Chronic motor tic disorder Is a True Chronic mental disorder Inferred relationship Some
Chronic schizophrenia Is a True Chronic mental disorder Inferred relationship Some
Recurrent conversion disorder Is a False Chronic mental disorder Inferred relationship Some
Intermittent explosive disorder Is a False Chronic mental disorder Inferred relationship Some
Recurrent major depression Is a False Chronic mental disorder Inferred relationship Some
poussée évolutive de schizophrénie latente chronique Is a False Chronic mental disorder Inferred relationship Some
Acute exacerbation of chronic schizoaffective schizophrenia Is a True Chronic mental disorder Inferred relationship Some
Chronic depression Is a True Chronic mental disorder Inferred relationship Some
Seasonal affective disorder (disorder) Is a False Chronic mental disorder Inferred relationship Some
Chronic alcoholic hepatitis Is a False Chronic mental disorder Inferred relationship Some
Recurrent manic episodes Is a False Chronic mental disorder Inferred relationship Some
Recurrent depression Is a False Chronic mental disorder Inferred relationship Some
Chronic organic mental disorder (disorder) Is a True Chronic mental disorder Inferred relationship Some
Chronic stress disorder (disorder) Is a True Chronic mental disorder Inferred relationship Some
Chronic psychogenic pain Is a True Chronic mental disorder Inferred relationship Some
Chronic depressive personality disorder Is a True Chronic mental disorder Inferred relationship Some
Chronic hypomanic personality disorder Is a True Chronic mental disorder Inferred relationship Some
Chronic harmful pattern of use of laxatives Is a False Chronic mental disorder Inferred relationship Some
Continuous chronic alcoholism Is a True Chronic mental disorder Inferred relationship Some
Episodic chronic alcoholism (disorder) Is a False Chronic mental disorder Inferred relationship Some
Chronic alcoholism in remission Is a True Chronic mental disorder Inferred relationship Some
Chronic bipolar II disorder, most recent episode major depressive Is a True Chronic mental disorder Inferred relationship Some
Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome is a rare, genetic, syndromic intellectual disability disorder characterized by severe intellectual disability, progressive, postnatal, multiple joint contractures and severe motor dysfunction. Patients present arrest and regression of motor function and speech acquisition, as well as contractures which begin in lower limbs and slowly progress in an ascending manner to include spine and neck, resulting in individuals presenting a specific fixed position. Is a False Chronic mental disorder Inferred relationship Some
A rare hereditary ataxia characterized by an early onset symptomatic generalized epilepsy, progressive cerebellar ataxia resulting in significant difficulties to walk or wheelchair dependency, and intellectual disability. Is a False Chronic mental disorder Inferred relationship Some
A rare, genetic, congenital muscular dystrophy due to dystroglycanopathy disorder characterized by a wide phenotypic spectrum which includes hypotonia and muscular weakness present at birth or early infancy and delayed or arrested motor development, associated with mild to severe intellectual disability and variable brain abnormalities on neuroimaging studies. Feeding difficulties, joint and spinal deformities, respiratory insufficiency, and ocular anomalies (e.g. strabismus, retinal dystrophy, oculomotor apraxia) may be associated. Decreased or absent alpha-dystroglycan on immunohistochemical muscle staining and elevated serum creatine kinase are observed. Is a False Chronic mental disorder Inferred relationship Some
A rare, fatal, inborn error of metabolism disorder characterized by respiratory distress and severe hypotonia at birth, severe global developmental delay, early-onset intractable seizures, myopathic facies with craniofacial dysmorphism (trigonocephaly/progressive microcephaly, low anterior hairline, arched eyebrows, hypotelorism, strabismus, small nose, prominent philtrum, thin upper lip, high-arched palate, micrognathia, malocclusion), severe, congenital flexion joint contractures and elevated serum creatine kinase levels. Scoliosis, optic atrophy, mild hepatomegaly, and hypoplastic genitalia may also be associated. Is a False Chronic mental disorder Inferred relationship Some
Epiphyseal dysplasia-hearing loss-dysmorphism syndrome is a rare multiple congenital anomalies/dysmorphic syndrome characterized by developmental delay, intellectual disability, short stature, sensorineural hearing impairment, facial dysmorphism (including epicanthus, broad, depressed nasal bridge, broad, fleshy nasal tip, mildly anteverted nares, deep nasolabial folds, broad mouth with thin upper lip) and skeletal anomalies (including abnormally placed thumbs, brachydactyly, scoliosis, dysplastic carpal bones). Patients also present severe behavior disturbances (aggression, hyperactivity), as well as hypopigmented skin lesions and hypoplastic digital patterns. There have been no further descriptions in the literature since 1992. Is a False Chronic mental disorder Inferred relationship Some
Brachydactyly-mesomelia-intellectual disability-heart defects syndrome is a rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by developmental delay, intellectual disability, thin habitus with narrow shoulders, mesomelic shortness of the arms, craniofacial dysmorphism (e.g. long lower face, maxillary hypoplasia, beak nose, short columella, prognathia, high arched palate, obtuse mandibular angle), brachydactyly (mostly involving middle phalanges) and cardiovascular anomalies (i.e. aortic root dilatation, mitral valve prolapse). Is a False Chronic mental disorder Inferred relationship Some
A rare congenital muscular alpha-dystroglycanopathy with brain and eye anomalies disease characterized by a severe muscle-eye-brain disease-like phenotype associated with intellectual disability, muscular dystrophy, macrocephaly and extended bilateral multicystic white matter disease. Is a False Chronic mental disorder Inferred relationship Some
Oppositional defiant disorder co-occurrent with chronic irritability-anger (disorder) Is a True Chronic mental disorder Inferred relationship Some
Neuronal ceroid lipofuscinosis 8 Is a False Chronic mental disorder Inferred relationship Some
Rett syndrome Is a True Chronic mental disorder Inferred relationship Some
Chronic post-traumatic stress disorder Is a True Chronic mental disorder Inferred relationship Some
A rare genetic disease characterized by mild intellectual deficit, congenital cataract, progressive sensorineural hearing impairment, ataxia, peripheral neuropathy, and short stature. There have been no further descriptions in the literature since 1991. Is a False Chronic mental disorder Inferred relationship Some
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly is a rare, central nervous system malformation syndrome characterized by progressive microcephaly with profound motor delay and intellectual disability, associated with hypertonia, spasticity, clonus, and seizures, with brain imaging revealing severe cerebral and cerebellar atrophy, and poor myelination. Is a False Chronic mental disorder Inferred relationship Some
Persistent depressive disorder is a chronic mood disorder characterized by persistent depressed mood present for a least two years, for most of the day and for more days than not. Is a True Chronic mental disorder Inferred relationship Some
Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome is a rare, genetic, neurodegenerative disease characterized by episodic metabolic encephalomyopathic crises (of variable frequency and severity which are frequently precipitated by an acute illness) which manifest with profound muscle weakness, ataxia, seizures, cardiac arrhythmias, rhabdomyolysis with myoglobinuria, elevated plasma creatine kinase, hypoglycemia, lactic acidosis, increased acylcarnitines and a disorientated or comatose state. Global developmental delay, intellectual disability and cortical, pyramidal and cerebellar signs develop with subsequent progressive neurodegeneration causing loss of expressive language and varying degrees of cerebral atrophy. Is a False Chronic mental disorder Inferred relationship Some
A rare, genetic, syndromic intellectual disability characterized by severe intellectual disability, non-inherited, progressive, post-natal microcephaly, hypotonia, hyperkinesia, absence of speech, strabismus, and midline stereotypic hand movements (e.g. hand washing/rubbing). Additional features include developmental delay, seizures and behavioral disturbances, such as self-injury and unexplained crying episodes. Is a False Chronic mental disorder Inferred relationship Some
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by moderate intellectual disability, dysmorphic facial features (such as prominent glabella, synophrys, and prognathism), generalized hirsutism, bilateral single palmar creases, and seizures. Additional reported manifestations include slowly progressive neurological deterioration with muscular weakness and impaired gait and balance, as well as hypogammaglobulinemia with specific absence of plasma and/or secretory IgA, among others. Brain imaging may show mild cerebellar atrophy and thin corpus callosum. Is a False Chronic mental disorder Inferred relationship Some
Spastic paraplegia-severe developmental delay-epilepsy syndrome is a rare, genetic, complex spastic paraplegia disorder characterized by an infantile-onset of psychomotor developmental delay with severe intellectual disability and poor speech acquisition, associated with seizures (mostly myoclonic), muscular hypotonia which may be noted at birth, and slowly progressive spasticity in the lower limbs leading to severe gait disturbances. Ocular abnormalities and incontinence are commonly associated. Other symptoms may include verbal dyspraxia, hypogenitalism, macrocephaly and sensorineural hearing loss, as well as dystonic movements and ataxia with upper limb involvement. Is a False Chronic mental disorder Inferred relationship Some
Allan-Herndon-Dudley syndrome Is a False Chronic mental disorder Inferred relationship Some
Spastic paraplegia-precocious puberty syndrome is a complex form of hereditary spastic paraplegia characterized by the onset of progressive spastic paraplegia associated with precocious puberty (due to Leydig cell hyperplasia) in childhood (at the age of 2 years). Moderate intellectual disability was also reported. There have been no further descriptions in the literature since 1983. Is a False Chronic mental disorder Inferred relationship Some
Spastic paraplegia-glaucoma-intellectual disability syndrome is characterized by progressive spastic paraplegia, glaucoma and intellectual deficit. It has been described in two families. The second described sibship was born to consanguineous parents. The mode of inheritance is autosomal recessive. Is a False Chronic mental disorder Inferred relationship Some
A rare complex hereditary spastic paraplegia characterized by an early onset hypotonia that progresses to spasticity, global developmental delay, severe intellectual disability and speech impairment, microcephaly, short stature and dysmorphic features. Patients often become non-ambulatory, and some develop seizures and stereotypic laughter. Is a False Chronic mental disorder Inferred relationship Some
A rare genetic neurological disorder characterized by postnatal microcephaly, hypotonia during infancy followed in most cases by progressive spasticity mainly affecting the lower limbs, and spastic diplegia or paraplegia, intellectual disability, delayed or absent speech, and dysarthria. Seizures and mildly dysmorphic features have been described in some patients. Is a False Chronic mental disorder Inferred relationship Some
A rare genetic neurological disorder characterized by progressive spastic paraparesis and delayed gross motor development with an onset in infancy or early childhood. Patients also show variable degrees of intellectual disability, speech delay, and dysarthria. Other reported features include microcephaly, seizures, bifid uvula with or without cleft palate, and ocular anomalies. Brain imaging shows white matter abnormalities in the periventricular and other regions. Is a False Chronic mental disorder Inferred relationship Some
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by global developmental delay and intellectual disability, progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, and dysmorphic craniofacial features (including microcephaly, hypertelorism, epicanthal folds, mild ptosis, strabismus, malar hypoplasia, short nose, depressed nasal bridge, full lips, small, low-set ears, and short neck). Craniosynostosis, generalized hypotonia, as well as asymmetry of the cerebral hemispheres and mild thinning of the corpus callosum on brain imaging have also been described. Is a False Chronic mental disorder Inferred relationship Some
Intellectual disability-spasticity-ectrodactyly syndrome is a rare intellectual disability syndrome characterized by severe intellectual disability, spastic paraplegia (with wasting of the lower limbs) and distal transverse defects of the limbs (e.g. ectrodactyly, syndactyly, clinodactyly of the hands and/or feet). Is a False Chronic mental disorder Inferred relationship Some
A rare multiple congenital anomalies/dysmorphic syndrome characterized by profound intellectual disability, choreoathetosis, progressive spastic diplegia, progressive tapetoretinal degeneration with loss of retinal vessels, and glomerulopathy resulting in death late in the first or early in the second decade of life. Absence of the cerebellar granular layer has been reported. There have been no further descriptions in the literature since 1982. Is a False Chronic mental disorder Inferred relationship Some
A rare genetic neurological disorder characterized by postnatal onset of severe global developmental delay, profound mental retardation, progressive microcephaly, progressive spasticity evolving into spastic quadriplegia with joint contractures, generalized seizures, and irritability. Severe choreoathetosis and dysmorphic features are absent. Brain imaging shows progressive cerebellar atrophy followed by cerebral atrophy affecting both white and gray matter, but no pontine involvement. Is a False Chronic mental disorder Inferred relationship Some
A rare leukodystrophy characterized by a spectrum of progressive neurologic manifestations comprising rapidly progressive early-onset nystagmus, spastic tetraplegia, and visual and hearing impairment, resulting in death in early childhood, as well as later onset of slowly progressive complex spastic ataxia with pyramidal and cerebellar symptoms and loss of developmental milestones. Brain imaging shows diffuse hypomyelination of the subcortical and deep white matter, cerebellar atrophy, and diffuse spinal cord volume loss. Is a False Chronic mental disorder Inferred relationship Some
A rare genetic, skeletal muscle disease with characteristics of early-onset hypotonia, muscle weakness, global developmental delay with intellectual disability and cardiomyopathy. Congenital structural heart defects and ichthyosiform cutaneous lesions have also been associated. Muscle biopsy shows characteristic enlarged mitochondria located at the periphery of muscle fibres. Is a False Chronic mental disorder Inferred relationship Some
A rare genetic syndromic intellectual disability characterised by global developmental delay, moderate to severe intellectual disability, motor and language impairment, behavioural abnormalities (with mood instability, aggression, and self-mutilation), and progressive hand tremor. Facial dysmorphism includes narrow palpebral fissures, large ears, long philtrum, and prominent chin. Is a True Chronic mental disorder Inferred relationship Some
Chronic harmful pattern of substance use Is a True Chronic mental disorder Inferred relationship Some
Psychosis co-occurrent and due to Parkinson's disease (disorder) Is a True Chronic mental disorder Inferred relationship Some

This concept is not in any reference sets

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