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: impulse control disorder (MONDO:0001162)
..Starting node ..kleptomania ()
Child Nodes:
Sister Nodes:
..intermittent explosive disorder ()
..kleptomania ()
..Kluver-Bucy syndrome ()
..pathological gambling ()
..primary polydipsia ()
..pyromania ()
..trichotillomania ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	1520
Name:	kleptomania
Definition:	A disorder characterized by the recurrent failure to resist the impulse to steal items of little intrinsic value; the individual experiences a rising subjective sense of tension before the theft and a sense of gratification or relief during the theft.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	kleptomania; pathological stealing
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes: KCNE3;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal