[
    {
        "diseaseId": 106,
        "name": "Autoimmune lymphoproliferative syndrome, type III; ALPS3",
        "description": "",
        "synonyms": [
            {
                "name": "Autoimmune lymphoproliferative syndrome"
            }
        ],
        "databaseLinks": [
            {
                "accession": "DOID:6688",
                "database": "Disease Ontology",
                "url": "http://purl.obolibrary.org/obo/DOID_6688",
                "species": "Human"
            },
            {
                "accession": "615559",
                "database": "OMIM",
                "url": "https://www.omim.org/entry/615559",
                "species": "Human"
            },
            {
                "accession": "ORPHA3261",
                "database": "Orphanet",
                "url": "http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=3261",
                "species": "Human"
            }
        ]
    },
    {
        "diseaseId": 107,
        "name": "Autoimmune lymphoproliferative syndrome with recurrent viral infections",
        "description": "",
        "synonyms": [
            {
                "name": "Autoimmune lymphoproliferative syndrome"
            },
            {
                "name": "Autoimmune lymphoproliferative syndrome, type IIB; ALPS2B"
            },
            {
                "name": "Caspase 8 deficiency"
            }
        ],
        "databaseLinks": [
            {
                "accession": "DOID:6688",
                "database": "Disease Ontology",
                "url": "http://purl.obolibrary.org/obo/DOID_6688",
                "species": "Human"
            },
            {
                "accession": "607271",
                "database": "OMIM",
                "url": "https://www.omim.org/entry/607271",
                "species": "Human"
            },
            {
                "accession": "ORPHA275517",
                "database": "Orphanet",
                "url": "http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=275517",
                "species": "Human"
            }
        ]
    },
    {
        "diseaseId": 108,
        "name": "Autoimmune lymphoproliferative syndrome, type IIA; ALPS2A",
        "description": "",
        "synonyms": [
            {
                "name": "Autoimmune lymphoproliferative syndrome"
            }
        ],
        "databaseLinks": [
            {
                "accession": "DOID:6688",
                "database": "Disease Ontology",
                "url": "http://purl.obolibrary.org/obo/DOID_6688",
                "species": "Human"
            },
            {
                "accession": "603909",
                "database": "OMIM",
                "url": "https://www.omim.org/entry/603909",
                "species": "Human"
            },
            {
                "accession": "ORPHA3261",
                "database": "Orphanet",
                "url": "http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=3261",
                "species": "Human"
            }
        ]
    },
    {
        "diseaseId": 977,
        "name": "Autoimmune lymphoproliferative syndrome; ALPS",
        "description": "ALPS covers a set of heterogenic heritable conditions characterised by a failure of apoptosis, that results in the accumulation of autoreactive lymphocytes. It manifests in early childhood as nonmalignant lymphadenopathy with hepatosplenomegaly and autoimmune cytopenias. Genes carrying ALPS-causing mutations include Fas receptor (type IA), fas ligand (type IB), caspase 10 (type IIA), caspase 8 (type IIB), PRKCD (ALPS3), NRAS (ALPS4) and CTLA4 (ALPS5).",
        "synonyms": [
        ],
        "databaseLinks": [
            {
                "accession": "DOID:6688",
                "database": "Disease Ontology",
                "url": "http://purl.obolibrary.org/obo/DOID_6688",
                "species": "Human"
            },
            {
                "accession": "601859",
                "database": "OMIM",
                "url": "https://www.omim.org/entry/601859",
                "species": "Human"
            },
            {
                "accession": "ORPHA3261",
                "database": "Orphanet",
                "url": "http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=3261",
                "species": "Human"
            }
        ]
    },
    {
        "diseaseId": 1145,
        "name": "Autoimmune lymphoproliferative syndrome, type V; ALPS5",
        "description": "",
        "synonyms": [
            {
                "name": "Autoimmune lymphoproliferative syndrome"
            },
            {
                "name": "CTLA4 haploinsuffiency with autoimmune infiltration; CHAI"
            }
        ],
        "databaseLinks": [
            {
                "accession": "DOID:6688",
                "database": "Disease Ontology",
                "url": "http://purl.obolibrary.org/obo/DOID_6688",
                "species": "Human"
            },
            {
                "accession": "616100",
                "database": "OMIM",
                "url": "https://www.omim.org/entry/616100",
                "species": "Human"
            }
        ]
    }
]