{
    "disease_id": "DOID:0111823",
    "recommended_name": {
        "id": "DOID:0111823",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111823",
        "name": "autosomal hemophilia A",
        "description": "A hemophilia characterized by autosomal inheritance of a Factor VIII deficiency."
    },
    "synonyms": [
        {
            "id": "DOID:0111823",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111823",
            "name": "autosomal Factor VIII deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010602",
            "name": "hemophilia A",
            "description": "The most common form of hemophilia characterized by spontaneous or prolonged hemorrhages due to factor VIII deficiency."
        },
        {
            "id": "MONDO:0010602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010602",
            "name": "congenital factor VIII disorder",
            "description": ""
        },
        {
            "id": "MONDO:0010602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010602",
            "name": "factor VIII deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010602",
            "name": "haemophilia a, X-linked recessive",
            "description": ""
        },
        {
            "id": "MONDO:0010602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010602",
            "name": "haemophilia type A",
            "description": ""
        },
        {
            "id": "MONDO:0010602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010602",
            "name": "haemophilia type a",
            "description": ""
        },
        {
            "id": "MONDO:0010602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010602",
            "name": "hemophilia A",
            "description": ""
        },
        {
            "id": "MONDO:0010602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010602",
            "name": "hemophilia a, X-linked recessive",
            "description": ""
        },
        {
            "id": "MONDO:0010602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010602",
            "name": "hemophilia type A",
            "description": ""
        },
        {
            "id": "MONDO:0010602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010602",
            "name": "hemophilia type a",
            "description": ""
        },
        {
            "id": "MONDO:0010602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010602",
            "name": "hereditary Factor VIII deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010602",
            "name": "hereditary Factor VIII deficiency disease",
            "description": ""
        },
        {
            "id": "MONDO:0010602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010602",
            "name": "HEMA",
            "description": ""
        },
        {
            "id": "MONDO:0010602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010602",
            "name": "Haemophilia A",
            "description": ""
        },
        {
            "id": "MONDO:0010602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010602",
            "name": "autosomal haemophilia a",
            "description": ""
        },
        {
            "id": "MONDO:0010602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010602",
            "name": "classic haemophilia",
            "description": ""
        },
        {
            "id": "MONDO:0010602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010602",
            "name": "classic hemophilia",
            "description": ""
        },
        {
            "id": "MONDO:0010602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010602",
            "name": "classical haemophilia",
            "description": ""
        },
        {
            "id": "MONDO:0010602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010602",
            "name": "classical hemophilia",
            "description": ""
        },
        {
            "id": "MONDO:0010602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010602",
            "name": "factor 8 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010602",
            "name": "haemophilia A, congenital",
            "description": ""
        },
        {
            "id": "MONDO:0010602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010602",
            "name": "hem A",
            "description": ""
        },
        {
            "id": "MONDO:0010602",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010602",
            "name": "hemophilia A, congenital",
            "description": ""
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111823"
    ],
    "unlinked_id_list": [],
    "crossref": [
        {
            "id": "DOID:0111823",
            "database": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111823",
            "categories": []
        },
        {
            "id": "MONDO:0010602",
            "database": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010602",
            "categories": []
        }
    ],
    "proteins": [
        {
            "uniprot_canonical_ac": "P00451-1",
            "uniprot_ac": "P00451",
            "uniprot_id": "FA8_HUMAN",
            "refseq_ac": "NP_000123",
            "glycoprotein": "yes",
            "species": [
                {
                    "name": "Homo sapiens",
                    "taxid": 9606,
                    "common_name": "Human",
                    "glygen_name": "Human",
                    "reference_species": "Homo sapiens [9606]"
                }
            ],
            "protein_names": [
                {
                    "name": "Coagulation factor VIII",
                    "type": "recommended"
                },
                {
                    "name": "AHF",
                    "type": "synonym"
                },
                {
                    "name": "Antihemophilic factor",
                    "type": "synonym"
                },
                {
                    "name": "Procoagulant component",
                    "type": "synonym"
                },
                {
                    "name": "antihemophilic factor",
                    "type": "synonym"
                },
                {
                    "name": "coagulation factor VIII A1 domain",
                    "type": "synonym"
                },
                {
                    "name": "coagulation factor VIII C2 domain",
                    "type": "synonym"
                },
                {
                    "name": "coagulation factor VIII isoform a preproprotein",
                    "type": "synonym"
                },
                {
                    "name": "coagulation factor VIII, procoagulant component",
                    "type": "synonym"
                },
                {
                    "name": "coagulation factor VIIIc",
                    "type": "synonym"
                },
                {
                    "name": "factor VIII F8B",
                    "type": "synonym"
                }
            ],
            "gene_names": [
                {
                    "name": "F8",
                    "type": "recommended"
                },
                {
                    "name": "AHF",
                    "type": "synonym"
                },
                {
                    "name": "DXS1253E",
                    "type": "synonym"
                },
                {
                    "name": "F8B",
                    "type": "synonym"
                },
                {
                    "name": "F8C",
                    "type": "synonym"
                },
                {
                    "name": "F8",
                    "type": "synonym"
                },
                {
                    "name": "FVIII",
                    "type": "synonym"
                },
                {
                    "name": "HEMA",
                    "type": "synonym"
                },
                {
                    "name": "THPH13",
                    "type": "synonym"
                }
            ],
            "record_id": "P00451-1",
            "evidence": [
                {
                    "id": "134500",
                    "database": "MIM",
                    "url": "https://www.omim.org/entry/134500"
                }
            ]
        },
        {
            "uniprot_canonical_ac": "K9M1U5-1",
            "uniprot_ac": "K9M1U5",
            "uniprot_id": "IFNL4_HUMAN",
            "refseq_ac": "NP_001263183",
            "glycoprotein": "no",
            "species": [
                {
                    "name": "Homo sapiens",
                    "taxid": 9606,
                    "common_name": "Human",
                    "glygen_name": "Human",
                    "reference_species": "Homo sapiens [9606]"
                }
            ],
            "protein_names": [
                {
                    "name": "Interferon lambda-4",
                    "type": "recommended"
                },
                {
                    "name": "IFN-lambda-4",
                    "type": "synonym"
                },
                {
                    "name": "interferon lambda-4 precursor",
                    "type": "synonym"
                },
                {
                    "name": "interferon, lambda 4",
                    "type": "synonym"
                }
            ],
            "gene_names": [
                {
                    "name": "IFNL4",
                    "type": "recommended"
                },
                {
                    "name": "IFNAN",
                    "type": "synonym"
                },
                {
                    "name": "IFNL4",
                    "type": "synonym"
                }
            ],
            "record_id": "K9M1U5-1",
            "evidence": [
                {
                    "id": "0111823",
                    "database": "AGR",
                    "url": "https://www.alliancegenome.org/disease/DOID:0111823"
                }
            ]
        }
    ],
    "glycans": [],
    "biomarkers": [],
    "association_flag": "1000",
    "record_id": "doid.0111823"
}