about
metachromatic leukodystrophyneurodegeneration with brain iron accumulationcerebral lipidosisspastic ataxia 3spastic ataxia 4spastic ataxia 5spinocerebellar ataxia type 38spinocerebellar ataxia type 28familial isolated deficiency of vitamin Eabetalipoproteinemiahereditary sensory neuropathy-deafness-dementia syndromeautosomal recessive cerebellar ataxia with late-onset spasticityrecessive mitochondrial ataxia syndromeautosomal recessive cerebellar ataxia due to a DNA repair defect
P279
Q1120682-004C5774-0394-453D-A6BD-42C5CB577748Q16892735-CAC3A14C-EF0C-438C-A9DC-8E3EBAFE5300Q18553924-E3B1A3AC-50B7-4D24-93F5-49E9CDE03D81Q21097758-E1DE6AD5-C937-4D37-8B14-7046AD99E579Q21097759-60AF9320-2A0F-47AD-B5C4-215AD21D0F01Q21097760-0EF248FD-5FFA-44FA-B94F-5AB6DF95FCAFQ21097780-0CC2887C-54FC-4C68-BFB2-3ACD6CF35BEAQ21097868-C5A9B941-3755-47F6-AFF5-C1D5BD31A342Q2868792-3364ADB8-D4D8-4767-8CE5-64C25AA87160Q319812-F99393D7-7FE3-4B04-87FE-F543BFD6FFA0Q50349724-7DD71A54-4D40-44EF-BE8E-CC6799114EB0Q55346025-A84987A1-37D3-4B2B-9387-6F302E2044E1Q55346085-F6CF93A9-57D0-49EF-B33F-6D4CD39159B1Q55346093-FBF71E6D-5CF1-4711-89A7-D7948E5B4DB2
P279
description
human disease
@en
name
démence d'origine métabolique
@fr
metabolic disease with dementia
@en
type
label
démence d'origine métabolique
@fr
metabolic disease with dementia
@en
altLabel
metabolic dementia
@en
prefLabel
démence d'origine métabolique
@fr
metabolic disease with dementia
@en
P1550
P2888
P5270
MONDO:0020142