{
    "disease_id": "DOID:0081269",
    "recommended_name": {
        "id": "DOID:0081269",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081269",
        "name": "pulmonary venoocclusive disease 2",
        "description": "A pulmonary venoocclusive disease that has_material_basis_in homozygous or compound heterozygous mutation in the EIF2AK4 gene on chromosome 15q15 and that is characterized histologically by widespread fibrous intimal proliferation of septal veins and preseptal venules, and is frequently associated with pulmonary capillary dilatation and proliferation."
    },
    "synonyms": [
        {
            "id": "DOID:0081269",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0081269",
            "name": "FAMILIAL PULMONARY CAPILLARY HEMANGIOMATOSIS",
            "description": ""
        },
        {
            "id": "MONDO:0009329",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009329",
            "name": "pulmonary venoocclusive disease 2",
            "description": "A rare form of pulmonary arterial hypertension (PAH) characterized by a capillary infiltration of the pulmonary interstitium, bronchioles and pleura leading to elevated pulmonary arterial resistance and right heart failure. PCH is potentially fatal."
        },
        {
            "id": "MONDO:0009329",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009329",
            "name": "pulmonary capillary hemangiomatosis",
            "description": ""
        },
        {
            "id": "MONDO:0009329",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009329",
            "name": "PVOD2",
            "description": ""
        },
        {
            "id": "MONDO:0009329",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009329",
            "name": "familial pulmonary capillary hemangiomatosis",
            "description": ""
        },
        {
            "id": "MONDO:0009329",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009329",
            "name": "pulmonary venoocclusive disease 2, autosomal recessive",
            "description": ""
        },
        {
            "id": "MIM:234810",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/234810",
            "name": "Pulmonary venoocclusive disease 2, autosomal recessive",
            "description": "Pulmonary venoocclusive disease 2, autosomal recessive"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081269"
    ],
    "unlinked_id_list": []
}