BMP15, bone morphogenetic protein 15, 9210

N. diseases: 48; N. variants: 18
Disease: Ovarian Dysgenesis 2 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1845294
Disease: Ovarian Dysgenesis 2
Ovarian Dysgenesis 2 		0.700 Biomarker disease GENOMICS_ENGLAND Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability. 26350204 2015
CUI: C1845294
Disease: Ovarian Dysgenesis 2
Ovarian Dysgenesis 2 		0.700 GeneticVariation disease UNIPROT Analyses of growth differentiation factor 9 (GDF9) and bone morphogenetic protein 15 (BMP15) mutation in Chinese women with premature ovarian failure. 19438907 2010
CUI: C1845294
Disease: Ovarian Dysgenesis 2
Ovarian Dysgenesis 2 		0.700 Biomarker disease GENOMICS_ENGLAND A novel BMP15 variant, potentially affecting the signal peptide, in a familial case of premature ovarian failure. 19486016 2009
CUI: C1845294
Disease: Ovarian Dysgenesis 2
Ovarian Dysgenesis 2 		0.700 GeneticVariation disease UNIPROT BMP15 mutations associated with primary ovarian insufficiency cause a defective production of bioactive protein. 19263482 2009
CUI: C1845294
Disease: Ovarian Dysgenesis 2
Ovarian Dysgenesis 2 		0.700 GeneticVariation disease UNIPROT Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure. 16645022 2006
CUI: C1845294
Disease: Ovarian Dysgenesis 2
Ovarian Dysgenesis 2 		0.700 GeneticVariation disease UNIPROT Identification of new variants of human BMP15 gene in a large cohort of women with premature ovarian failure. 16464940 2006
CUI: C1845294
Disease: Ovarian Dysgenesis 2
Ovarian Dysgenesis 2 		0.700 GeneticVariation disease UNIPROT Missense mutations in the BMP15 gene are associated with ovarian failure. 16508750 2006
CUI: C1845294
Disease: Ovarian Dysgenesis 2
Ovarian Dysgenesis 2 		0.700 GeneticVariation disease UNIPROT Hypergonadotropic ovarian failure associated with an inherited mutation of human bone morphogenetic protein-15 (BMP15) gene. 15136966 2004
CUI: C1845294
Disease: Ovarian Dysgenesis 2
Ovarian Dysgenesis 2 		0.700 CausalMutation disease CLINVAR
CUI: C1845294
Disease: Ovarian Dysgenesis 2
Ovarian Dysgenesis 2 		0.700 Biomarker disease CTD_human