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        "title": "Divergent structure of the human synexin (annexin VII) gene and assignment to chromosome 10.",
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    {
        "title": "Expression and prognostic relevance of annexin A3 in prostate cancer.",
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        "date": "2008",
        "authors": "Kollermann J, Schlomm T, Bang H, Schwall GP, von Eichel-Streiber C, Simon R, Schostak M, Huland H, Berg W, Sauter G, Klocker H, Schrattenholz A",
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                        "EHBP1 familial prostate cancer",
                        "familial prostate cancer caused by mutation in EHBP1",
                        "prostate cancer, hereditary, type 12",
                        "HPC12",
                        "prostate cancer, hereditary, 13",
                        "MSMB familial prostate cancer",
                        "familial prostate cancer caused by mutation in MSMB",
                        "prostate cancer, hereditary, type 13",
                        "HPC13",
                        "prostate cancer, hereditary, 11",
                        "HPC11",
                        "prostate cancer, hereditary, 14",
                        "HPC14",
                        "prostate cancer, hereditary, 15",
                        "HPC15",
                        "prostate cancer, hereditary",
                        "Prostate cancer, hereditary, 1",
                        "Prostate cancer, hereditary, 9",
                        "Prostate cancer, hereditary, 12",
                        "Prostate cancer, hereditary, 13",
                        "Prostate cancer, hereditary, 11",
                        "Prostate cancer"
                    ],
                    "id_list": [
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        "title": "Chromosomal localization of the human annexin III (ANX3) gene.",
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                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009815",
                                "name": "osteopetrosis autosomal recessive 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009815",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009815",
                                "name": "osteopetrosis infantile malignant 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009815",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009815",
                                "name": "osteopetrosis, autosomal recessive 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011877",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011877",
                                "name": "autosomal dominant osteopetrosis 1",
                                "description": "Autosomal dominant osteopetrosis type I (ADO I) is a sclerosing bone disorder characterized by skeletal densification that predominantly involves the cranial vault."
                            },
                            {
                                "id": "MONDO:0011877",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011877",
                                "name": "LRP5 osteopetrosis (disease)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011877",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011877",
                                "name": "OPTA1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011877",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011877",
                                "name": "autosomal dominant osteopetrosis type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011877",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011877",
                                "name": "osteopetrosis (disease) caused by mutation in LRP5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011877",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011877",
                                "name": "osteopetrosis, autosomal dominant type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011877",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011877",
                                "name": "osteopetrosis autosomal dominant type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011877",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011877",
                                "name": "osteopetrosis, autosomal dominant 1",
                                "description": ""
                            },
                            {
                                "id": "MIM:259700",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/259700",
                                "name": "Osteopetrosis, autosomal recessive 1",
                                "description": "Osteopetrosis, autosomal recessive 1"
                            },
                            {
                                "id": "MIM:607634",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/607634",
                                "name": "Osteopetrosis, autosomal dominant 1",
                                "description": "Osteopetrosis, autosomal dominant 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "13533",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:13533"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111411",
                        "recommended_name": {
                            "id": "DOID:0111411",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0111411",
                            "name": "exudative vitreoretinopathy 4",
                            "description": "An exudative vitreoretinopathy that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the LRP5 gene on chromosome 11q13.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111411",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0111411",
                                "name": "EVR4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011151",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011151",
                                "name": "exudative vitreoretinopathy 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011151",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011151",
                                "name": "exudative vitreoretinopathy 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011151",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011151",
                                "name": "exudative vitreoretinopathy type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011151",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011151",
                                "name": "EVR4",
                                "description": ""
                            },
                            {
                                "id": "MIM:601813",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/601813",
                                "name": "Vitreoretinopathy, exudative 4",
                                "description": "Vitreoretinopathy, exudative 4"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "601813",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/601813"
                            },
                            {
                                "id": "0111411",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0111411"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0060849",
                        "recommended_name": {
                            "id": "DOID:0060849",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0060849",
                            "name": "osteoporosis-pseudoglioma syndrome",
                            "description": "A syndrome characterized by congenital or infancy-onset blindness, very low bone mass, decreased trabecular bone volume, severe juvenile-onset osteoporosis and spontaneous fractures, pseudoglioma, microphthalmia that has_material_basis_in homozygous or compound heterozygous mutation in the LRP5 gene on chromosome 11q13."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0060849",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0060849",
                                "name": "OPPG",
                                "description": ""
                            },
                            {
                                "id": "DOID:0060849",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0060849",
                                "name": "ocular form of osteogenesis imperfecta",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009820",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009820",
                                "name": "osteoporosis-pseudoglioma syndrome",
                                "description": "Osteoporosis pseudoglioma syndrome is a very rare autosomal recessive disorder characterized by congenital or infancy-onset blindness and severe juvenile-onset osteoporosis and spontaneous fractures."
                            },
                            {
                                "id": "MONDO:0009820",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009820",
                                "name": "OPPG",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009820",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009820",
                                "name": "osteoporosis-pseudoglioma syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009820",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009820",
                                "name": "osteogenesis imperfecta ocular form",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009820",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009820",
                                "name": "osteoporosis pseudoglioma syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009820",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009820",
                                "name": "pseudoglioma with bone fragility",
                                "description": ""
                            },
                            {
                                "id": "MIM:259770",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/259770",
                                "name": "Osteoporosis-pseudoglioma syndrome",
                                "description": "Osteoporosis-pseudoglioma syndrome"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "259770",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/259770"
                            },
                            {
                                "id": "0060849",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0060849"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0060980",
                        "recommended_name": {
                            "id": "DOID:0060980",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0060980",
                            "name": "polycystic liver disease 1",
                            "description": "A polycystic disease characterized by the presence of multiple liver cysts of biliary epithelial origin that has_material_basis_in heterozygous mutation in the PRKCSH gene on chromosome 19p13."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008265",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008265",
                                "name": "polycystic liver disease 1",
                                "description": "A polycystic liver disease in which the cause of the disease is a mutation in the PRKCSH gene, and is characterized by the appearance of numerous cysts spread throughout the liver."
                            },
                            {
                                "id": "MONDO:0008265",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008265",
                                "name": "isolated congenital polycystic liver disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008265",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008265",
                                "name": "isolated polycystic liver disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008265",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008265",
                                "name": "PCLD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008265",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008265",
                                "name": "nonsyndromic congenital polycystic liver disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008265",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008265",
                                "name": "nonsyndromic polycystic liver disease (disease)",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008265",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008265",
                                "name": "polycystic liver disease 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008265",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008265",
                                "name": "polycystic liver disease 1 with or without kidney cysts",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008265",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008265",
                                "name": "ADPCLD",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008265",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008265",
                                "name": "PCLD",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008265",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008265",
                                "name": "isolated autosomal dominant polycystic liver disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008265",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008265",
                                "name": "polycystic liver disease",
                                "description": ""
                            },
                            {
                                "id": "MIM:174050",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/174050",
                                "name": "Polycystic liver disease 1 with or without kidney cysts",
                                "description": "Polycystic liver disease 1 with or without kidney cysts"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0060980",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0060980"
                            },
                            {
                                "id": "0060980",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0060980"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0060977",
                        "recommended_name": {
                            "id": "DOID:0060977",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0060977",
                            "name": "polycystic liver disease 4",
                            "description": "A liver disease characterized by adult-onset of liver cysts arising from the bile duct epithelium that has_material_basis_in heterozygous mutation in the LRP5 gene on chromosome 11q13."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0044327",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0044327",
                                "name": "polycystic liver disease 4 with or without kidney cysts",
                                "description": "An autosomal dominant disease characterized by adult-onset of liver cysts arising from the bile duct epithelium, caused by heterozygous mutation in the LRP5 gene. Some patients may develop a few kidney cysts, but these are often incidental and do not result in renal failure."
                            },
                            {
                                "id": "MONDO:0044327",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0044327",
                                "name": "polycystic liver disease 4 with or without kidney cysts",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0044327",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0044327",
                                "name": "PCLD4",
                                "description": ""
                            },
                            {
                                "id": "MIM:617875",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/617875",
                                "name": "Polycystic liver disease 4 with or without kidney cysts",
                                "description": "Polycystic liver disease 4 with or without kidney cysts"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "617875",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/617875"
                            },
                            {
                                "id": "0060977",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0060977"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0080037",
                        "recommended_name": {
                            "id": "DOID:0080037",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080037",
                            "name": "Worth syndrome",
                            "description": "A hyperostosis that has_material_basis_in a mutation in the LRP5 gene which results_in increased bone density and bony structures located_in palate."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0080037",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0080037",
                                "name": "autosomal dominant endosteal hyperostosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:0080037",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0080037",
                                "name": "autosomal dominant osteosclerosis",
                                "description": ""
                            },
                            {
                                "id": "DOID:0080037",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0080037",
                                "name": "benign form of Worth hyperostosis corticalis generalisata with torus platinus",
                                "description": ""
                            },
                            {
                                "id": "DOID:0080037",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0080037",
                                "name": "Worth's syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007764",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007764",
                                "name": "autosomal dominant osteosclerosis, Worth type",
                                "description": "A sclerozing bone disorder characterized by generalized skeletal densification, particularly of the cranial vault and tubular long bones, which is not associated to an increased risk of fracture."
                            },
                            {
                                "id": "MONDO:0007764",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007764",
                                "name": "Ostosclrose autosomique dominante type Worth",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007764",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007764",
                                "name": "Worth syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007764",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007764",
                                "name": "Worth's syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007764",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007764",
                                "name": "endosteal hyperostosis, Worth type",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007764",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007764",
                                "name": "hyperostosis, endosteal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007764",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007764",
                                "name": "VBCH2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007764",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007764",
                                "name": "Van Buchem disease type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007764",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007764",
                                "name": "hyperostosis corticalis generalisata, benign form of Worth with torus palatinus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007764",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007764",
                                "name": "osteosclerosis of the skull and enlarged mandible",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007764",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007764",
                                "name": "osteosclerosis, autosomal dominant, Worth type",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007764",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007764",
                                "name": "autosomal dominant osteosclerosis, Worth type",
                                "description": "A sclerozing bone disorder characterized by generalized skeletal densification, particularly of the cranial vault and tubular long bones, which is not associated to an increased risk of fracture."
                            },
                            {
                                "id": "MONDO:0007764",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007764",
                                "name": "Ostosclrose autosomique dominante type Worth",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007764",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007764",
                                "name": "Worth syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007764",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007764",
                                "name": "Worth's syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007764",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007764",
                                "name": "endosteal hyperostosis, Worth type",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007764",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007764",
                                "name": "hyperostosis, endosteal",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007764",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007764",
                                "name": "VBCH2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007764",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007764",
                                "name": "Van Buchem disease type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007764",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007764",
                                "name": "hyperostosis corticalis generalisata, benign form of Worth with torus palatinus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007764",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007764",
                                "name": "osteosclerosis of the skull and enlarged mandible",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007764",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007764",
                                "name": "osteosclerosis, autosomal dominant, Worth type",
                                "description": ""
                            },
                            {
                                "id": "MIM:144750",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/144750",
                                "name": "Endosteal hyperostosis, Worth type",
                                "description": "Endosteal hyperostosis, Worth type"
                            },
                            {
                                "id": "MIM:607636",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/607636",
                                "name": "Van Buchem disease 2",
                                "description": "Van Buchem disease 2"
                            }
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