MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation portal

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

*:HP: HPO terms, ND: NAMDC terms.
Most Studied CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO

Disease Browser
Parent Node: dissociative disorder (MONDO:0001160)
..Starting node ..dissociative amnesia ()
Child Nodes:
Sister Nodes:
..depersonalization disorder ()
..dissociative amnesia ()
..multiple personality disorder ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	1185
Name:	dissociative amnesia
Definition:	A disorder characterized by a retrospective gap in memory of important personal information, usually of a traumatic or stressful nature; the memory loss far exceeds ordinary forgetfulness and is not the result of substance use or the consequence of a medical condition.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	psychogenic amnesia
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes: PTCH1; PTCH2; SUFU;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal