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78689005: Chronic brain syndrome (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
130571014 Chronic brain syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
130574018 Chronic encephalopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
819656010 Chronic brain syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
130571014 Chronic brain syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
130571014 Chronic brain syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
130574018 Chronic encephalopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
130574018 Chronic encephalopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
819656010 Chronic brain syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
819656010 Chronic brain syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4647091000241116 encéphalopathie chronique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4647091000241116 encéphalopathie chronique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

139 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Chronic brain syndrome (disorder) Is a syndrome cérébral non spécifique false Inferred relationship Existential restriction modifier (core metadata concept)
Chronic brain syndrome (disorder) Is a Chronic nervous system disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Chronic brain syndrome (disorder) Finding site Brain structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Chronic brain syndrome (disorder) Course Chronic (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept)
Chronic brain syndrome (disorder) Clinical course Chronic (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Chronic brain syndrome (disorder) Is a Disorder of brain true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Chronic alcoholic brain syndrome Is a False Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Chronic brain-hydrocephalus syndrome Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Chronic non-psychotic brain syndrome (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Paroxysmal dystonia Is a False Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Persistent vegetative state (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
épilepsie partielle complexe récidivante Is a False Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Frequent episodic tension-type headache (disorder) Is a False Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Chronic progressive non-hereditary chorea Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
PEHO-like syndrome is a rare, genetic neurological disease characterised by progressive encephalopathy, early-onset seizures with a hypsarrhythmic pattern, facial and limb oedema, severe hypotonia, early arrest of psychomotor development and craniofacial dysmorphism (evolving microcephaly, narrow forehead, short nose, prominent auricles, open mouth, micrognathia), in the absence of neuro-ophthalmic or neuroradiologic findings. Poor visual responsiveness, growth failure and tapering fingers are also associated. Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
épilepsie partielle continue progressive chronique Is a False Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A rare multiple congenital anomalies syndrome characterized by cutaneous mastocytosis, microcephaly, microtia and/or hearing loss, hypotonia and skeletal anomalies (e.g. clinodactyly, camptodactyly, scoliosis). Additional common features are short stature, intellectual disability and difficulties. Facial dysmorphism may include upslanted palpebral fissures, highly arched palate and micrognathia. Rarely, seizures and asymmetrically small feet have been reported. Is a False Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Chronic viral encephalitis Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Chronic organic mental disorder (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Chronic anoxic encephalopathy Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Chronic intractable migraine without aura (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Recurrent benign focal seizures of childhood Is a False Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Intermittent cerebral ischaemia Is a False Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Intermittently raised pressure hydrocephalus Is a False Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Myoclonic epilepsy with ragged red fibers (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Huntington disease-like 3 Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Progressive polyneuropathy with bilateral striatal necrosis (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Fatal post-viral neurodegenerative disorder Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A rare neurodegenerative disease characterized by slowly progressive ataxia, amyotrophy of the hands and distal arms, spastic paraplegia, progressive sensorineural hearing loss, hypogonadism and short stature. Additional features include generalized cerebellar atrophy and peripheral nervous system anomalies. Small cervical spinal cord, intellectual/language disability and localized vitiligo have also been reported. There have been no further descriptions in the literature since 1989. Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A rare genetic neurological disorder characterized by childhood to adolescent-onset of action myoclonus, generalized tonic-clonic seizures and slowly progressive, moderate to severe cognitive impairment that may lead to dementia. EEG reveals progressive slowing of background activity and epileptic abnormalities and brain MRI shows cerebellar and brainstem atrophy. There is evidence the disease may be caused by homozygous mutation in the CERS1 gene on chromosome 19p12. Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Progressive myoclonic epilepsy type 3 (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A rare hereditary cerebellar ataxia disorder with characteristics of late-onset spinocerebellar ataxia, manifesting with slowly progressive gait disturbances, dysarthria, limb and truncal ataxia and smooth-pursuit eye movement disturbance, associated with a history of psychomotor delay from childhood. Mild atrophy of the cerebellar vermis and hemispheres is observed on brain imaging. There is evidence the disease is caused by homozygous mutation in the SYT14 gene on chromosome 1q32. Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A rare genetic neurological disorder characterised by early-onset progressive ataxia associated with myoclonic seizures (frequently associated with other seizure types such as generalised tonic-clonic, absence and drop attacks), scoliosis of variable severity, areflexia, elevated creatine kinase serum levels and relative preservation of cognitive function until late in the disease course. There is evidence the disease is caused by homozygous mutation in the GOSR2 gene on chromosome 17q21. Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A rare genetic neurological disorder characterised by early-onset progressive ataxia associated with myoclonic seizures, generalised tonic-clonic seizures (which are often sleep-related) and normal to mild intellectual disability. Dysarthria, upward gaze palsy, sensory neuropathy, developmental delay and autistic disorder have also been associated. Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Cranio-cervical dystonia with laryngeal and upper limb involvement (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital muscular dystrophy with intellectual disability (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Walker-Warburg congenital muscular dystrophy Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital muscular dystrophy with cerebellar involvement Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A rare fatal inborn error of metabolism disorder with characteristics of 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. There is evidence the disease is caused by homozygous or compound heterozygous mutation in the DPM2 gene on chromosome 9q34. Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Infantile osteopetrosis with neuroaxonal dysplasia syndrome (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Thoracic dysplasia and hydrocephalus syndrome (disorder) Is a False Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Epiphyseal dysplasia, microcephalus, nystagmus syndrome Is a False Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A rare genetic autosomal recessive cerebellar ataxia disease with characteristics of slowly progressive spinocerebellar ataxia developing during childhood, manifesting with gait and limb ataxia, postural tremor, dysarthria, sensory alterations (for example decreased vibration sense), eye movement anomalies (such as nystagmus, saccadic pursuit, oculomotor apraxia), upper and lower limb fasciculations and hyperreflexia with Babinski signs. Brain imaging reveals cerebellar, pontine, vermian and medullar atrophy. There is evidence the disease is caused by compound heterozygous mutation in the TPP1 gene on chromosome 11p15. Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Adult-onset autosomal recessive cerebellar ataxia (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Muscle eye brain disease with bilateral multicystic leukodystrophy Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Huntington's chorea Is a False Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Non-Alzheimer's progressive dysphasia Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Semantic dementia Is a False Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Progressive aphasia (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Mitochondrial neurogastrointestinal encephalomyopathy syndrome (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Progressive external ophthalmoplegia, myopathy, emaciation syndrome Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A rare neuronal ceroid lipofuscinosis disorder with characteristics of juvenile-onset progressive spinocerebellar ataxia, bulbar syndrome (manifesting with dysarthria, dysphagia and dysphonia), pyramidal and extrapyramidal involvement (including myoclonus, amyotrophy, unsteady gait, akinesia, rigidity, dysarthric speech) and intellectual deterioration. Muscle biopsy displays autofluorescent bodies and lipofuscin deposits in brain and occasionally the retina upon post mortem. Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Progressive focal cortical atrophy Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
X-linked progressive cerebellar ataxia (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Van Bogaert's sclerosing leukoencephalitis Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Rett syndrome Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary cerebral amyloid angiopathy, Icelandic type Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Boucher Neuhäuser syndrome Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Parkinsonian syndrome with idiopathic orthostatic hypotension (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Progressive cerebellar ataxia with hypogonadism Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Syndrome with characteristics of congenital cerebellar hypoplasia, endosteal sclerosis, hypotonia, ataxia, mild to moderate developmental delay, short stature, hip dislocation, and tooth eruption disturbances. It has been described in four patients. Less common manifestations are microcephaly, strabismus, nystagmus, optic atrophy and dysarthria. It is appears to be transmitted as an autosomal recessive trait. Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A rare late-onset neurodegenerative disease with characteristics of supranuclear gaze palsy, postural instability, progressive rigidity, and mild dementia. Five clinical variants have been described with clinicopathological correlations, with Richardson's syndrome the most common clinical variant. The disease has neuropathological manifestations of neuronal loss, gliosis with astrocytic plaques and accumulation of tau-immunoreactive neurofibrillary tangles in specific brain areas. The differences in the rate and areas of accumulation of phosphorylated tau protein correlate with the five clinical variants. The disease is a 4R tauopathy composed of a preponderance of four-repeat (exon 10 positive) tau isoforms and a characteristic biochemical profile (doublet tau 64 and tau 69). The MAPT H1-clade specific sub-haplotype, H1c, is a risk factor for this disease. Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Progressive post hemorrhagic ventricular dilatation Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Childhood-onset basal ganglia degeneration syndrome Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome (disorder) Is a False Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A rare genetic cerebral small vessel disease characterized by recurrent ischemic strokes, often with a predilection for the pons, with typical onset in the fourth or fifth decade of life. Patients present progressive cognitive and motor impairment with pyramidal, bulbar, and cerebellar symptoms, among others. Brain imaging shows multiple lacunar infarcts, typically with involvement of the pons, as well as variable leukoencephalopathy of the cerebral hemispheres. Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Spastic paraplegia, severe developmental delay, epilepsy syndrome (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Chronic bilirubin encephalopathy Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Severe oculo-renal-cerebellar syndrome (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Familial infantile bilateral striatal necrosis Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Progressive cerebello-cerebral atrophy (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Spinocerebellar ataxia type 42 Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Spinocerebellar ataxia type 41 (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Spinocerebellar ataxia type 43 Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Inosine triphosphate pyrophosphohydrolase-related lethal infantile neurological disorder with cataract and cardiac involvement (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Disease with characteristics of progressive ataxia beginning during infancy, a pyramidal syndrome and dental agenesis. The syndrome has been described in four children born to consanguineous parents. The mode of transmission is autosomal recessive. Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Progressive myoclonic epilepsy type 7 Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Progressive congenital rubella encephalomyelitis Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Postpartum amenorrhoea-galactorrhea syndrome Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Cerebellar ataxia with oculomotor apraxia type 4 Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A rare genetic neurological disorder characterized by infantile onset of progressive leukoencephalopathy, microcephaly, severe global developmental delay, and spasticity resulting in quadriparesis and posture deformation. Additional features include an abnormally exaggerated startle reflex, seizures, dystonia, and hypomimia or amimia, as well as progressive chest deformities and contractures of large and hyperextensibility of small joints, among others. Thin corpus callosum is a prominent feature in brain imaging, in addition to white matter abnormalities consistent with leukoencephalopathy. Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Early-onset calcifying leucoencephalopathy, skeletal dysplasia Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Progressive myoclonic epilepsy type 9 Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Corticobasal syndrome (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Mitochondrial enoyl coenzyme A reductase protein-associated neurodegeneration syndrome (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
PYCR2-related microcephaly, progressive leucoencephalopathy Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Chronic cluster headache Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis, parkinsonism, dementia complex of Kii Peninsula Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Amyotrophic lateral sclerosis, parkinsonism, dementia complex of West New Guinea (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Paroxysmal choreoathetosis (disorder) Is a False Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Birnbaum's syndrome (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Friedreich ataxia (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Spinocerebellar ataxia type 46 (disorder) Is a True Chronic brain syndrome (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

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