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CCNO and infertility are reported together in 1 article.
Gene
CCNO
- HGNC
- HGNC:18576
3articles
3mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
Phenotype
Infertility
199articles
199mentions
12co-reported genes shown
Most co-reported genes (articles)
Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.
Publications
1 records shown · first 60A genomics approach to females with infertility and recurrent pregnancy loss.
PMID 32172300 | DOI 10.1007/s00439-020-02143-5 · Human genetics · 2020 · 17 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | CCNO | “Candidate variants in genes linked to primary ciliary dyskinesia (DNAH11 and CCNO) were identified in individuals with and without systemic features of the disease.” | 0.98 | hgnc_dict_v1 |
| phenotype | infertility | “A genomics approach to females with infertility and recurrent pregnancy loss.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | TLE6 | “These include variants in previously established female infertility-related genes (TLE6, NLRP7, FSHR, and ZP1) as well as genes with only tentative links in the literature (NLRP5).” | 0.98 | hgnc_dict_v1 |
| gene | NLRP7 | “These include variants in previously established female infertility-related genes (TLE6, NLRP7, FSHR, and ZP1) as well as genes with only tentative links in the literature (NLRP5).” | 0.98 | hgnc_dict_v1 |