{"database":"EVA","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Vcf":["ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB39694/CHH_project_NGS_data_only.vcf.gz.tbi","ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB39694/CHH_project_NGS_data_only.vcf.gz","ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB39694/CHH_project_Sanger_sequencing_data_only.vcf.gz.tbi","ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB39694/CHH_project_Sanger_sequencing_data_only.vcf.gz"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"dataset_type":["Genotyping By Sequencing, Whole Genome Sequencing"],"omics_type":["Genomics"],"submitter":["The Cyprus Institute of Neurology and Genetics"],"instrument_platform":["Illumina NextSeq 500"],"species":["Homo Sapiens"],"full_dataset_link":["https://www.ebi.ac.uk/eva/?eva-study=PRJEB39694"],"repository":["EVA"],"name_synonyms":["HH12, Lhrh1, 5-oxoPro-His-Trp-Ser-Tyr-Gly-Leu-Arg-Pro-Gly-NH2 (human or pig), Gnrh2, Cystorelin, LHFSH, familial, LHRH, FSH-Releasing Hormone, Luliberin, LFRH, FSH Releasing Hormone, Gnrha, LNRH, GnRH, Gnrh, Rgnrhg1, Dirigestran, Kryptocur, hpg, genetic, Releasing Hormone, Gonadotropin Releasing Hormone, LHFSHRH, LH FSH Releasing Hormone, Gn-RH, Gonadoliberin, Gonadorelin Acetate., Luteinizing Hormone-Releasing Hormone, Luteinizing Hormone Releasing Hormone, Gonadorelin Hydrochloride, Factrel, LH-Releasing Hormone, inherited genetic, LH-FSH Releasing Hormone, LHFSH Releasing Hormone, Gonadorelin, Lhrh, LH-RH, constitutitional genetic, hereditary, GNRH, GRH, Lnrh, LH Releasing Hormone"],"additional_accession":[]},"is_claimable":false,"name":"Genetic etiologies of GnRH deficiency","description":"Pathogenic variants implicated in Congenital Hypogonadotropic Hypogonadism","dates":{"publication":"2020-08-07"},"accession":"PRJEB39694","cross_references":{"TAXONOMY":["9606"]}}