{
    "disease_id": "DOID:0050817",
    "recommended_name": {
        "id": "DOID:0050817",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0050817",
        "name": "Stargardt disease",
        "description": "An age related macular degeneration that is characterized by progressive vision loss usually to the point of legal blindness."
    },
    "synonyms": [
        {
            "id": "DOID:0050817",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050817",
            "name": "STARGARDT DISEASE 1",
            "description": ""
        },
        {
            "id": "MONDO:0009549",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009549",
            "name": "severe early-childhood-onset retinal dystrophy",
            "description": "Severe early childhood onset retinal dystrophy (SECORD) is an inherited retinal dystrophy (see this term), characterized by a severe congenital night blindness, progressive retinal dystrophy and nystagmus. Best corrected visual acuity can reach 0.3 in the first decade of life and can pertain well into the second decade of life. Blindness is often complete by the age of 30 years. An overlap with Leber congenital amaurosis (LCA; see this term) occurs when patients are characterized by their visual acuity and panretinal dystrophy."
        },
        {
            "id": "MONDO:0009549",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009549",
            "name": "SECORD",
            "description": ""
        },
        {
            "id": "MONDO:0009549",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009549",
            "name": "fundus flavimaculatus",
            "description": ""
        },
        {
            "id": "MONDO:0009549",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009549",
            "name": "macular Degeneration, juvenile",
            "description": ""
        },
        {
            "id": "MONDO:0009549",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009549",
            "name": "EOSRD",
            "description": ""
        },
        {
            "id": "MONDO:0009549",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009549",
            "name": "Stargardt disease type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009549",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009549",
            "name": "early-onset severe retinal dystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0009549",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009549",
            "name": "Stgd",
            "description": ""
        },
        {
            "id": "MONDO:0009549",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009549",
            "name": "retinal dystrophy, early-onset severe",
            "description": ""
        },
        {
            "id": "MONDO:0009549",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009549",
            "name": "STGD1",
            "description": ""
        },
        {
            "id": "MONDO:0009549",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009549",
            "name": "Stargardt disease 1",
            "description": ""
        },
        {
            "id": "MONDO:0009549",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009549",
            "name": "Stargardt disease 1; STGD1",
            "description": ""
        },
        {
            "id": "MONDO:0009549",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009549",
            "name": "macular dystrophy with flecks, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0011370",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011370",
            "name": "Stargardt disease 4",
            "description": "Any Stargardt disease in which the cause of the disease is a mutation in the PROM1 gene."
        },
        {
            "id": "MONDO:0011370",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011370",
            "name": "Stargardt disease 4",
            "description": ""
        },
        {
            "id": "MONDO:0011370",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011370",
            "name": "Stargardt disease type 4",
            "description": ""
        },
        {
            "id": "MONDO:0011370",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011370",
            "name": "Stargardt disease caused by mutation in PROM1",
            "description": ""
        },
        {
            "id": "MONDO:0011370",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011370",
            "name": "STGD4",
            "description": ""
        },
        {
            "id": "MONDO:0011370",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011370",
            "name": "Stargardt disease 4; STGD4",
            "description": ""
        },
        {
            "id": "MONDO:0011370",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011370",
            "name": "PROM1 Stargardt disease",
            "description": ""
        },
        {
            "id": "MONDO:0010819",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010819",
            "name": "Stargardt disease 3",
            "description": ""
        },
        {
            "id": "MONDO:0010819",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010819",
            "name": "Stargardt disease 3",
            "description": ""
        },
        {
            "id": "MONDO:0010819",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010819",
            "name": "Stargardt disease type 3",
            "description": ""
        },
        {
            "id": "MONDO:0010819",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010819",
            "name": "STGD3",
            "description": ""
        },
        {
            "id": "MONDO:0010819",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010819",
            "name": "macular dystrophy with flecks, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0010819",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010819",
            "name": "Stargardt disease 3; STGD3",
            "description": ""
        },
        {
            "id": "MONDO:0010819",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010819",
            "name": "Stargardt-like macular dystrophy, autosomal dominant",
            "description": ""
        },
        {
            "id": "MIM:248200",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/248200",
            "name": "Stargardt disease 1",
            "description": "Stargardt disease 1"
        },
        {
            "id": "MIM:603786",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/603786",
            "name": "Stargardt disease 4",
            "description": "Stargardt disease 4"
        },
        {
            "id": "MIM:600110",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/600110",
            "name": "Stargardt disease 3",
            "description": "Stargardt disease 3"
        }
    ]
}