MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation portal

Hello! Guest! Please Login or Register! Clinician Mode

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: anomaly of puberty or/and menstrual cycle (MONDO:0015860)
Parent Node: primary ovarian failure (MONDO:0005387)
..Starting node ..acquired primary ovarian failure ()
Child Nodes:
Sister Nodes:
..acquired primary ovarian failure ()
..autoimmune primary ovarian failure ()
..inherited primary ovarian failure ()
..premature menopause ()
..premature ovarian failure 10 ()
..premature ovarian failure 13 ()
..premature ovarian failure 14 ()
..premature ovarian failure 15 ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	19851
Name:	acquired primary ovarian failure
Definition:	An instance of primary ovarian failure that is acquired during the lifetime of the individual.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	acquired premature ovarian failure; acquired primary ovarian failure
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal