Other specified degenerative diseases of nervous system

Preferred Label : Other specified degenerative diseases of nervous system;

Is an underlying disease (dagger code) : true;

Diag associé à un acte (%) : 76.7;

CMA : 2;

Source : OMS;

Date de début : 01/01/1997;

Date de mise à jour : 01/01/2016;

Details

Origin ID

G318;

UMLS CUI

C0477365;

DO Cross reference
- Aicardi-Goutieres syndrome [DO Concept]
Orphanet concepts
- Acute necrotizing encephalopathy of childhood [ORDO Disease]
- Aicardi-Goutières syndrome [ORDO Disease]
- Allan-Herndon-Dudley syndrome [ORDO Disease]
- Alpers-Huttenlocher syndrome [ORDO Disease]
- Argyrophilic grain disease [ORDO Disease]
- Autosomal dominant striatal neurodegeneration [ORDO Disease]
- Autosomal recessive cerebral atrophy [ORDO Disease]
- Childhood-onset basal ganglia degeneration syndrome [ORDO Disease]
- Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder [ORDO Disease]
- Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type [ORDO Disease]
- Dementia with Lewy body [ORDO Disease]
- Early-onset calcifying leukoencephalopathy-skeletal dysplasia [ORDO Disease]
- Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome [ORDO Disease]
- Early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome [ORDO Disease]
- Familial encephalopathy with neuroserpin inclusion bodies [ORDO Disease]
- Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome [ORDO Disease]
- Leigh syndrome [ORDO Disease]
- Leigh syndrome with cardiomyopathy [ORDO Disease]
- Leigh syndrome with leukodystrophy [ORDO Disease]
- Leigh syndrome with nephrotic syndrome [ORDO Disease]
- Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome [ORDO Disease]
- Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy [ORDO Disease]
- NAD(P)HX dehydratase deficiency [ORDO Disease]
- Neurodegenerative syndrome due to cerebral folate transport deficiency [ORDO Disease]
- PEHO syndrome [ORDO Disease]
- PEHO-like syndrome [ORDO Disease]
- PRKAR1B-related neurodegenerative dementia with intermediate filaments [ORDO Disease]
- Perry syndrome [ORDO Disease]
- Primary progressive apraxia of speech [ORDO Disease]
- Primary progressive freezing gait [ORDO Disease]
- Progressive cerebello-cerebral atrophy [ORDO Disease]
- Progressive encephalopathy with leukodystrophy due to DECR deficiency [ORDO Disease]
- Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome [ORDO Disease]
- Severe neurodegenerative syndrome with lipodystrophy [ORDO Disease]
- Sporadic Leigh syndrome [ORDO Disease]
- Sporadic adult-onset ataxia of unknown etiology [ORDO Disease]
- X-linked intellectual disability-ataxia-apraxia syndrome [ORDO Disease]
- X-linked neurodegenerative syndrome, Bertini type [ORDO Disease]
- X-linked neurodegenerative syndrome, Hamel type [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients