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                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, protection against, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, resistance to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant lung neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant lung tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant lung tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant neoplasm of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant neoplasm of the lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumor of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumor of the lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumour of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumour of the lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "nonsmall cell lung cancer, response to tyrosine kinase inhibitor in, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "nonsmall cell lung cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "nonsmall cell lung cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "lung cancer susceptibility 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "LNCR1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "lung cancer susceptibility",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "lung cancer susceptibility 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012942",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                                "name": "lung cancer susceptibility 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012942",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                                "name": "LNCR3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012942",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                                "name": "lung cancer susceptibility 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012955",
                                "name": "lung cancer susceptibility 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012955",
                                "name": "LNCR4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012955",
                                "name": "lung cancer susceptibility 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013631",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013631",
                                "name": "lung cancer susceptibility 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013631",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013631",
                                "name": "LNCR5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013631",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013631",
                                "name": "lung cancer susceptibility 5",
                                "description": ""
                            },
                            {
                                "id": "MIM:211980",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/211980",
                                "name": "Lung cancer",
                                "description": "Lung cancer"
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:4765"
                        ],
                        "evidence": [
                            {
                                "id": "1324",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:1324"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2531",
                        "recommended_name": {
                            "id": "DOID:2531",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:2531",
                            "name": "hematologic cancer",
                            "description": "An organ system cancer located in the hematological system that is characterized by uncontrolled cellular proliferation in blood, bone marrow and lymph nodes."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2531",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:2531",
                                "name": "Hematologic malignancy",
                                "description": ""
                            },
                            {
                                "id": "DOID:2531",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:2531",
                                "name": "Hematologic neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:2531",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:2531",
                                "name": "Hematological tumors",
                                "description": ""
                            },
                            {
                                "id": "DOID:2531",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:2531",
                                "name": "blood cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:2531",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:2531",
                                "name": "hematopoietic and lymphoid system tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:2531",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:2531",
                                "name": "hematopoietic cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:2531",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:2531",
                                "name": "hematopoietic neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:2531",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:2531",
                                "name": "hematopoietic tumors",
                                "description": ""
                            },
                            {
                                "id": "DOID:2531",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:2531",
                                "name": "malignant hematopoietic neoplasm",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:0081452",
                            "DOID:706",
                            "DOID:1039",
                            "DOID:5604",
                            "DOID:6536",
                            "DOID:0080638",
                            "DOID:7757",
                            "DOID:0050743",
                            "DOID:4960",
                            "DOID:8527",
                            "DOID:1036",
                            "DOID:5772"
                        ],
                        "evidence": [
                            {
                                "id": "2531",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2531"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0110873",
                        "recommended_name": {
                            "id": "DOID:0110873",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0110873",
                            "name": "holoprosencephaly 9",
                            "description": "A holoprosencephaly that has_material_basis_in heterozygous mutation in the GLI2 gene on chromosome 2q14."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0110873",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110873",
                                "name": "pituitary anomalies with holoprosencephaly-like features",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110873",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110873",
                                "name": "HPE9",
                                "description": ""
                            },
                            {
                                "id": "DOID:0110873",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0110873",
                                "name": "holoprosencephaly with microphthalmia and first branchial arch anomalies",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012563",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012563",
                                "name": "holoprosencephaly 9",
                                "description": "Any holoprosencephaly in which the cause of the disease is a mutation in the GLI2 gene."
                            },
                            {
                                "id": "MONDO:0012563",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012563",
                                "name": "GLI2 holoprosencephaly",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012563",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012563",
                                "name": "HPE9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012563",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012563",
                                "name": "holoprosencephaly 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012563",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012563",
                                "name": "holoprosencephaly caused by mutation in GLI2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012563",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012563",
                                "name": "holoprosencephaly type 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012563",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012563",
                                "name": "holoprosencephaly with microphthalmia and first branchial arch anomalies",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012563",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012563",
                                "name": "pituitary anomalies with holoprosencephaly-like features",
                                "description": ""
                            },
                            {
                                "id": "MIM:610829",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/610829",
                                "name": "Holoprosencephaly 9",
                                "description": "Holoprosencephaly 9"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "610829",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/610829"
                            },
                            {
                                "id": "0110873",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0110873"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0080776",
                        "recommended_name": {
                            "id": "DOID:0080776",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080776",
                            "name": "partial androgen insensitivity syndrome",
                            "description": "An androgen insensitivity syndrome that is characterized by a 46,XY karyotype and testes that produce age-appropriate androgen levels but have undermasculinized external genitalia due to defects in androgen action."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0080776",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0080776",
                                "name": "Reifenstein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "partial androgen insensitivity syndrome",
                                "description": "Partial androgen insensitivity syndrome (PAIS) is a disorder of sex development (DSD) distinct from complete AIS (CAIS) characterized by the presence of abnormal genital development in a 46,XY individual with normal testis development and partial responsiveness to age-appropriate levels of androgens."
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "PAIS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "Reifenstein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "Reifenstein syndrome, partial",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "androgen insensitivity, partial",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "androgen insensitivity, partial, with or without breast cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "androgen insensitivity, partial, with or without breast cancer, X-linked recessive",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "familial incomplete Male pseudohermaphroditism, type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "pais",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "partial androgen resistance syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "pseudohermaphroditism, incomplete male, type I",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "androgen insensitivity syndrome, partial",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "androgen resistance syndrome, partial",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "incomplete male pseudohermaphroditism",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "type I familial incomplete male pseudohermaphroditism",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "partial androgen insensitivity syndrome",
                                "description": "Partial androgen insensitivity syndrome (PAIS) is a disorder of sex development (DSD) distinct from complete AIS (CAIS) characterized by the presence of abnormal genital development in a 46,XY individual with normal testis development and partial responsiveness to age-appropriate levels of androgens."
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "PAIS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "Reifenstein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "Reifenstein syndrome, partial",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "androgen insensitivity, partial",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "androgen insensitivity, partial, with or without breast cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "androgen insensitivity, partial, with or without breast cancer, X-linked recessive",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "familial incomplete Male pseudohermaphroditism, type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "pais",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "partial androgen resistance syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "pseudohermaphroditism, incomplete male, type I",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "androgen insensitivity syndrome, partial",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "androgen resistance syndrome, partial",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "incomplete male pseudohermaphroditism",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "type I familial incomplete male pseudohermaphroditism",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010720",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "partial androgen insensitivity syndrome",
                                "description": "Partial androgen insensitivity syndrome (PAIS) is a disorder of sex development (DSD) distinct from complete AIS (CAIS) characterized by the presence of abnormal genital development in a 46,XY individual with normal testis development and partial responsiveness to age-appropriate levels of androgens."
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                            },
                            {
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                            {
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                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "androgen insensitivity, partial, with or without breast cancer, X-linked recessive",
                                "description": ""
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                                "url": "https://monarchinitiative.org/disease/MONDO:0010720",
                                "name": "familial incomplete Male pseudohermaphroditism, type 1",
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                                "name": "pseudohermaphroditism, incomplete male, type I",
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                                "url": "https://monarchinitiative.org/disease/MONDO:0014369",
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