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    {
        "title": "Characterization of the human nasal embryonic LHRH factor gene, NELF, and a mutation screening among 65 patients with idiopathic hypogonadotropic hypogonadism (IHH).",
        "journal": "Journal of human genetics",
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        "authors": "Miura K, Acierno JS Jr, Seminara SB",
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                            "description": "A hypogonadotropic hypogonadism that is characterized by autosomal dominant inheritance and has_material_basis_in heterozygous mutation in the NELF gene on chromosome 9q34, sometimes in association with mutation in another gene."
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                                "id": "MONDO:0013911",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013911",
                                "name": "hypogonadotropic hypogonadism 9 with or without anosmia",
                                "description": "Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the NSMF gene."
                            },
                            {
                                "id": "MONDO:0013911",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013911",
                                "name": "NSMF hypogonadotropic hypogonadism",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013911",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013911",
                                "name": "hypogonadotropic hypogonadism 9 with or without anosmia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013911",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013911",
                                "name": "hypogonadotropic hypogonadism caused by mutation in NSMF",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013911",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013911",
                                "name": "HH9",
                                "description": ""
                            },
                            {
                                "id": "MIM:614838",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/614838",
                                "name": "Hypogonadotropic hypogonadism 9 with or without anosmia",
                                "description": "Hypogonadotropic hypogonadism 9 with or without anosmia"
                            }
                        ],
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                                "url": "https://www.omim.org/entry/614838"
                            },
                            {
                                "id": "0090085",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090085"
                            }
                        ]
                    }
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        "title": "NELF is a nuclear protein involved in hypothalamic GnRH neuronal migration.",
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        "authors": "Xu N, Bhagavath B, Kim HG, Halvorson L, Podolsky RS, Chorich LP, Prasad P, Xiong WC, Cameron RS, Layman LC",
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