{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009097", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009097", 
            "name": "persistent hyperplastic primary vitreous, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009097", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009097", 
            "name": "retinal nonattachment, nonsyndromic congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009097", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009097", 
            "name": "retinal nonattachment and falciform detachment"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009097", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009097", 
            "name": "autosomal recessive persistent hyperplastic primary vitreous"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009097", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009097", 
            "name": "PHPVAR"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009097", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009097", 
            "name": "persistent fetal vasculature"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009097", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009097", 
            "name": "persistent hyperplastic primary vitreous, autosomal recessive; PHPVAR"
        }, 
        {
            "url": "https://www.omim.org/entry/221900", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:221900", 
            "name": "Persistent hyperplastic primary vitreous, autosomal recessive"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060282", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060282", 
        "name": "persistent hyperplastic primary vitreous"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/221900", 
            "id": "221900", 
            "database": "MIM"
        }
    ]
}