A progressive neurological disease defined by specific neuropathological features associating brainstem and basal ganglia lesions.
Synonyms:
Infantile subacute necrotizing encephalopathy
Leigh disease
This is just here as a test because I lose it
Term information
database
cross reference
- UMLS:C0023264 (E (Exact mapping: the two concepts are equivalent))
- ICD-10:G31.8 (- NTBT (ORPHA code's Narrower Term maps to a Broader Term). - Index term (The ORPHA code is listed in the ICD Index).)
- OMIM:256000 (E (Exact mapping: the two concepts are equivalent))
- MeSH:D007888 (E (Exact mapping: the two concepts are equivalent))
- MedDRA:10062950 (E (Exact mapping: the two concepts are equivalent))
- ICD-11:5C53.24 (- E (Exact mapping: the two concepts are equivalent). - Specific code (The ORPHA code has its own code in the ICD).)
- UMLS:C0751267 (E (Exact mapping: the two concepts are equivalent))
definition citation
- Orphanet
expertlink
- https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=506
hasDbXref
- MeSH:D007888
- OMIM:256000
- UMLS:C0751267
- ICD-11:5C53.24
- MedDRA:10062950
- UMLS:C0023264
- ICD-10:G31.8
has age of onset
- http://www.orpha.net/ORDO/Orphanet_409950
has annual incidence range
- http://www.orpha.net/ORDO/Orphanet_409977
has birth prevalence range
- http://www.orpha.net/ORDO/Orphanet_409977
has inheritance
- http://www.orpha.net/ORDO/Orphanet_409930
- http://www.orpha.net/ORDO/Orphanet_409933
- http://www.orpha.net/ORDO/Orphanet_409932
has point prevalence range
- http://www.orpha.net/ORDO/Orphanet_409981
- http://www.orpha.net/ORDO/Orphanet_409977
notation
- Clinical group
present in
- http://www.orpha.net/ORDO/Orphanet_409984
- http://www.orpha.net/ORDO/Orphanet_409991
- http://www.orpha.net/ORDO/Orphanet_410006