MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
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Disease Browser
Parent Node:
expandprimary ovarian failure (MONDO:0005387)
..Starting node
..expandpremature ovarian failure 14 ()

       Child Nodes:



 Sister Nodes: 
..expandacquired primary ovarian failure ()
..expandautoimmune primary ovarian failure ()
..expandinherited primary ovarian failure ()
..expandpremature menopause ()
..expandpremature ovarian failure 10 ()
..expandpremature ovarian failure 13 ()
..expandpremature ovarian failure 14 ()
..expandpremature ovarian failure 15 ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Could not execute query 3
SELECT t5.Variation_Name, t5.GeneID, t5.GeneSymbol, t5.ClinicalSignificance, t5.dbSNP, t5.RCVaccession, t5.TestedInGTR, t5.PhenotypeIDs, t5.Chromosome, t5.Start, t5.Stop, t5.HGVS_c, t5.HGVS_p, t5.HGVS_g, t5.OtherIDs, t5.Diseases as Disease_ClinVar FROM gb_exome.clinvar_variation_v2_latest as t5 WHERE Assembly ='GRCh37' AND (t5.PhenotypeIDs like '%:618014%' OR t5.otherIDs like '%OMIM Allelic Variant:618014%' ) ORDER by GeneSymbol, t5.ClinicalSignificance LIKE 'Patho%' DESC, t5.ClinicalSignificance LIKE '%likely pathog%' DESC, start <1,start;
Term ID:44777
Name:premature ovarian failure 14
Definition:
Alternative IDs:618014
ParentIDs:
TreeNumbers:
Synonyms:GDF9-related primary ovarian insufficiency; POF14; premature ovarian failure 14; POF14
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM: 618014;
MSeqDR LSDB:  
Genes: