{
    "disease_id": "DOID:0060282",
    "recommended_name": {
        "id": "DOID:0060282",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060282",
        "name": "persistent hyperplastic primary vitreous",
        "description": "A developmental vitreous disease that is characterized by leukocoria, strabismus and vision loss, caused by failure of primary vitreous and hyaloid vasculature to regress during embryological development."
    },
    "synonyms": [
        {
            "id": "MONDO:0012653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012653",
            "name": "PHPVAD",
            "description": ""
        },
        {
            "id": "MONDO:0012653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012653",
            "name": "persistent hyperplastic primary vitreous, autosomal dominant; PHPVAD",
            "description": ""
        },
        {
            "id": "MONDO:0012653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012653",
            "name": "PHPVAD",
            "description": ""
        },
        {
            "id": "MONDO:0012653",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012653",
            "name": "persistent hyperplastic primary vitreous, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0009097",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009097",
            "name": "persistent hyperplastic primary vitreous, autosomal recessive",
            "description": "Autosomal recessive form of persistent hyperplastic primary vitreous."
        },
        {
            "id": "MONDO:0009097",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009097",
            "name": "retinal nonattachment, nonsyndromic congenital",
            "description": ""
        },
        {
            "id": "MONDO:0009097",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009097",
            "name": "retinal nonattachment and falciform detachment",
            "description": ""
        },
        {
            "id": "MONDO:0009097",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009097",
            "name": "autosomal recessive persistent hyperplastic primary vitreous",
            "description": ""
        },
        {
            "id": "MONDO:0009097",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009097",
            "name": "PHPVAR",
            "description": ""
        },
        {
            "id": "MONDO:0009097",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009097",
            "name": "persistent fetal vasculature",
            "description": ""
        },
        {
            "id": "MONDO:0009097",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009097",
            "name": "persistent hyperplastic primary vitreous, autosomal recessive; PHPVAR",
            "description": ""
        },
        {
            "id": "MONDO:0009097",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009097",
            "name": "persistent hyperplastic primary vitreous, autosomal recessive",
            "description": ""
        },
        {
            "id": "MIM:221900",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/221900",
            "name": "Persistent hyperplastic primary vitreous, autosomal recessive",
            "description": "Persistent hyperplastic primary vitreous, autosomal recessive"
        }
    ]
}