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288547000: Ability to perform functions related to communication (observable entity)

Status: current, Not 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
428210010 Ability to perform functions related to communication en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
682894015 Ability to perform functions related to communication (observable entity) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2536132011 Communication ability en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
117301000077110 capacité d'exécuter les fonctions reliées à la communication fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

60 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Ability to perform functions related to communication Is a Ability to perform activities of everyday life false Inferred relationship Some
Ability to perform functions related to communication Is a Communication speech and language observable (observable entity) true Inferred relationship Some
Ability to perform functions related to communication Is a Ability to perform function / activity true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Dysphasia as late effect of cerebrovascular disease Interprets True Ability to perform functions related to communication Inferred relationship Some 3
Speech and language deficit due to and following embolic cerebrovascular accident (disorder) Interprets False Ability to perform functions related to communication Inferred relationship Some 3
Articulation disorder due to hyperkinesis (disorder) Interprets True Ability to perform functions related to communication Inferred relationship Some 2
Spastic dysphonia Interprets True Ability to perform functions related to communication Inferred relationship Some 2
Dysphonia of Gilles de la Tourette's syndrome Interprets True Ability to perform functions related to communication Inferred relationship Some 2
Speech and language deficit due to and following hemorrhagic cerebrovascular accident (disorder) Interprets False Ability to perform functions related to communication Inferred relationship Some 3
Voice disorder due to psychosexual conflict Interprets True Ability to perform functions related to communication Inferred relationship Some 2
Dysphonia of palatopharyngolaryngeal myoclonus Interprets True Ability to perform functions related to communication Inferred relationship Some 5
Fluency disorder due to and following cerebrovascular accident (disorder) Interprets False Ability to perform functions related to communication Inferred relationship Some 3
Acquired language comprehension impairment (disorder) Interprets True Ability to perform functions related to communication Inferred relationship Some 3
Velopharyngeal mislearning Interprets True Ability to perform functions related to communication Inferred relationship Some 2
Acquired dysphasia (disorder) Interprets False Ability to perform functions related to communication Inferred relationship Some 3
Psychogenic dysphonia Interprets False Ability to perform functions related to communication Inferred relationship Some 2
Disorder of language Interprets True Ability to perform functions related to communication Inferred relationship Some 1
Pervasive developmental disorder with marked impairment of functional language without loss of previously acquired skills (disorder) Interprets True Ability to perform functions related to communication Inferred relationship Some 3
Pervasive developmental disorder with impairment of functional language (disorder) Interprets True Ability to perform functions related to communication Inferred relationship Some 3
Pervasive developmental disorder with marked impairment of functional language with loss of previously acquired skills (disorder) Interprets True Ability to perform functions related to communication Inferred relationship Some 3
Pervasive developmental disorder with disorder of intellectual development and pervasive impairment of functional language without loss of previously acquired skills (disorder) Interprets True Ability to perform functions related to communication Inferred relationship Some 4
Pervasive developmental disorder with disorder of intellectual development and marked impairment of functional language with loss of previously acquired skills Interprets True Ability to perform functions related to communication Inferred relationship Some 4
Pervasive developmental disorder with disorder of intellectual development and marked impairment of functional language without loss of previously acquired skills Interprets True Ability to perform functions related to communication Inferred relationship Some 4
Pervasive developmental disorder with disorder of intellectual development and complete impairment of functional language without loss of previously acquired skills (disorder) Interprets True Ability to perform functions related to communication Inferred relationship Some 4
Pervasive developmental disorder with disorder of intellectual development and absence of functional language with loss of previously acquired skills (disorder) Interprets True Ability to perform functions related to communication Inferred relationship Some 4
Pervasive developmental disorder with disorder of intellectual development and complete impairment of functional language with loss of previously acquired skills Interprets True Ability to perform functions related to communication Inferred relationship Some 4
Pervasive developmental disorder with severe impairment of functional language with loss of previously acquired skills (disorder) Interprets True Ability to perform functions related to communication Inferred relationship Some 3
Pervasive developmental disorder with severe impairment of functional language without loss of previously acquired skills (disorder) Interprets True Ability to perform functions related to communication Inferred relationship Some 3
Ability to use augmentative and alternative communication Is a True Ability to perform functions related to communication Inferred relationship Some
Pervasive developmental disorder with abscence of functional language (disorder) Interprets True Ability to perform functions related to communication Inferred relationship Some 3
Pervasive developmental disorder with complete impairment of functional language with loss of previously acquired skills Interprets True Ability to perform functions related to communication Inferred relationship Some 3
Pervasive developmental disorder with complete impairment of functional language without loss of previously acquired skills (disorder) Interprets True Ability to perform functions related to communication Inferred relationship Some 3
Pervasive developmental disorder with complete impairment of functional language (disorder) Interprets True Ability to perform functions related to communication Inferred relationship Some 3
Pervasive developmental disorder with cognitive developmental delay and complete impairment of functional language (disorder) Interprets True Ability to perform functions related to communication Inferred relationship Some 4
Pervasive developmental disorder with cognitive developmental delay and marked impairment of functional language (disorder) Interprets True Ability to perform functions related to communication Inferred relationship Some 4
Post-traumatic mutism Interprets True Ability to perform functions related to communication Inferred relationship Some 6
Acquired dysphasia (disorder) Interprets True Ability to perform functions related to communication Inferred relationship Some 2
Foreign accent syndrome is a rare motor speech disorder characterized by a speech pattern that results in accent changes perceived as new and different to their native accent. The etiology is unclear but occurs most commonly following structural neurological damage e.g. cerebrovascular accident but has also been associated with a functional neurological etiology. Interprets True Ability to perform functions related to communication Inferred relationship Some 1
A rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by moderate to severe intellectual disability, developmental delay, macrocephaly, speech delay, and hypotonia. Dysmorphic facial features include a high, broad, and/or prominent forehead, laterally sparse eyebrows, widely spaced and deeply-set eyes, narrow palpebral fissures, low-set ears, full/prominent cheeks, midface hypoplasia, thin upper lip, and a pointed chin. Additional variable manifestations include joint laxity, abnormality of vision (including hypermetropia, strabismus, and cerebral visual impairment), genital abnormalities in males, and inguinal, umbilical, or hiatal hernia. Interprets True Ability to perform functions related to communication Inferred relationship Some 2
Psychogenic dysphonia Interprets True Ability to perform functions related to communication Inferred relationship Some 1
X-linked intellectual disability-short stature-overweight syndrome is a multiple congenital anomalies syndrome characterised by borderline to severe intellectual disability, speech delay, short stature, elevated body mass index, a pattern of truncal obesity (reported in older males), and variable neurologic features (e.g. hypotonia, tremors, gait disturbances, behavioural problems, and seizure disorders). Less common manifestations include microcephaly, microorchidism and/or microphallus. Dysmorphic features have been reported in some patients but no consistent pattern has been noted. Interprets True Ability to perform functions related to communication Inferred relationship Some 4
A rare multiple congenital anomalies/dysmorphic syndrome characterized by developmental delay, severe intellectual disability, severe speech and communication problems and distinctive dysmorphic faces (high hairline, thin eyebrows, hypertelorism, dysmorphic ears, broad nasal bridge and tip, and narrow jaw). Height is not affected. Some patients may also present autistic behaviors. Interprets True Ability to perform functions related to communication Inferred relationship Some 4
A rare multiple congenital anomalies/dysmorphic syndrome with characteristics of developmental delay, speech delay and variable degree of intellectual disability (mostly mid-to-moderate but some patients may also have normal intelligence) due to CHD4 gene mutations. Even though clinical manifestations are significantly variable among patients, most patients manifest dysmorphic facial features (could sometimes include macrocephaly), congenital heart defects, hypotonia and ophthalmologic abnormalities. Other clinical features may include brain structure anomalies, skeletal anomalies, hearing impairment and gonadal abnormalities. Interprets True Ability to perform functions related to communication Inferred relationship Some 4
A rare genetic intellectual disability syndrome characterized by global developmental delay, intellectual disability, severe speech delay, behavioral abnormalities (including impulsivity, compulsivity, stubbornness, manipulative behaviors, temper tantrums, and aggressive behaviors), autism spectrum disorder and mild and variable dysmorphic facies (including deep-set eyes and a prominent nasal septum, extending below the alae nasi) due to point mutation of USP7 gene or 16p13.2 microdeletion where USP7 is completely or partially deleted. Behavioral abnormalities are more pronounced in microdeletion. Patients may also have hypotonia, feeding problems, delayed walking with unsteady gait, hypogonadism in males, seizures and ocular anomalies (such as myopia, esotropia, strabismus, and nystagmus). Interprets True Ability to perform functions related to communication Inferred relationship Some 4
A partial deletion of the short arm of chromosome 16 characterized by developmental delay, intellectual disability, speech delay, autism spectrum disorder, epilepsy, hypogonadism, and hypotonia. The behavioral profile includes impulsivity, compulsivity, stubbornness, manipulative behaviors, temper tantrums, and aggressive behaviors. Interprets True Ability to perform functions related to communication Inferred relationship Some 6
A rare syndromic intellectual disability without congenital anomalies/specific dysmorphic phenotype characterised by delayed psychomotor development, severe intellectual disability, delayed or absent speech development, hypotonia, ataxic gait and feeding difficulties. Clinical symptoms are evident from early infancy. Majority of the patients also present with behavioural abnormalities (including autistic features, aggressive behaviour, low frustration tolerance, and stereotypies such as hand-flapping). Additional clinical features may include inability to walk, seizures, hearing loss, sleep abnormalities, joint hyperlaxity. Nonspecific dysmorphic facial features (small head, strabismus, epicanthal folds, synophrys, high palate, low-set ears, orofacial hypotonia, full eyelids, and eversion of the lower lip) may also be present. Interprets True Ability to perform functions related to communication Inferred relationship Some 3
A rare neurologic disease characterized by impaired ability to execute complex coordinated movements underlying the production of speech, leading to highly unintelligible speech in the absence of muscular or sensory deficits. Interprets True Ability to perform functions related to communication Inferred relationship Some 1

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