MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO
Disease Browser
Parent Node:
expandAlzheimer disease (MONDO:0004975)
Parent Node:
expandgenetic neurodegenerative disease with dementia (MONDO:0021037)
..Starting node
..expandearly-onset autosomal dominant Alzheimer disease ()

       Child Nodes:
........expandAlzheimer disease 10 ()
........expandAlzheimer disease 11 ()
........expandAlzheimer disease 12 ()
........expandAlzheimer disease 13 ()
........expandAlzheimer disease 14 ()
........expandAlzheimer disease 15 ()
........expandAlzheimer disease 2 ()
........expandAlzheimer disease 3 ()
........expandAlzheimer disease 4 ()
........expandAlzheimer disease 5 ()
........expandAlzheimer disease 6 ()
........expandAlzheimer disease 7 ()
........expandAlzheimer disease 8 ()
........expandAlzheimer disease type 1 ()
........expandAlzheimer disease, familial early-onset, with Coexisting amyloid and prion pathology ()



 Sister Nodes: 
..expandataxia with dementia ()
..expandcorticobasal syndrome ()
..expandearly-onset autosomal dominant Alzheimer disease ()
..expandfrontotemporal dementia ()
..expandfrontotemporal dementia with motor neuron disease ()
..expandhereditary sensory neuropathy-deafness-dementia syndrome ()
..expandHuntington disease ()
..expandHuntington disease-like syndrome due to C9ORF72 expansions ()
..expandinherited prion disease ()
..expandITM2B amyloidosis ()
..expandneuroacanthocytosis ()
..expandneurodegeneration with brain iron accumulation ()
..expandPRKAR1B-related neurodegenerative dementia with intermediate filaments ()
..expandprogressive supranuclear palsy ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:15140
Name:early-onset autosomal dominant Alzheimer disease
Definition:Early-onset autosomal dominant Alzheimer disease (EOAD) is a progressive dementia with reduction of cognitive functions. EOAD presents the same phenotype as sporadic Alzheimer disease (AD) but has an early age of onset, usually before 60 years old.
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Synonyms:early-onset familial autosomal dominant Alzheimer disease; early-onset, autosomal dominant Alzheimer disease; EOFAD; familial Alzheimer disease
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal