{
    "disease_id": "DOID:0061157",
    "recommended_name": {
        "id": "DOID:0061157",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061157",
        "name": "retinopathy sensory neuropathy syndrome",
        "description": "A syndrome characterized by progressive visual impairment due to retinopathy (usually retinitis pigmentosa) and progressive sensory neuropathy resulting in distal sensory loss of various modalities (vibration, proprioception, pain) that has_material_basis_inhomozygous or compound heterozygous mutation in the FLVCR1 gene on chromosome 1q32."
    },
    "synonyms": [
        {
            "id": "DOID:0061157",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061157",
            "name": "PCARP",
            "description": ""
        },
        {
            "id": "DOID:0061157",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061157",
            "name": "Posterior Column Ataxia with Retinitis Pigmentosa",
            "description": ""
        },
        {
            "id": "DOID:0061157",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061157",
            "name": "posterior column ataxia-retinitis pigmentosa syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0012177",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012177",
            "name": "posterior column ataxia-retinitis pigmentosa syndrome",
            "description": "Posterior column ataxia - retinitis pigmentosa is characterized by the association of progressive sensory ataxia and retinitis pigmentosa."
        },
        {
            "id": "MONDO:0012177",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012177",
            "name": "PCARP",
            "description": ""
        },
        {
            "id": "MONDO:0012177",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012177",
            "name": "ataxia, posterior column, with retinitis pigmentosa",
            "description": ""
        },
        {
            "id": "MONDO:0012177",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012177",
            "name": "autosomal recessive posterior column ataxia and retinitis pigmentosa",
            "description": ""
        },
        {
            "id": "MONDO:0012177",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012177",
            "name": "AXPC1",
            "description": ""
        },
        {
            "id": "MONDO:0012177",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012177",
            "name": "POSTERIOR column ataxia with retinitis pigmentosa",
            "description": ""
        },
        {
            "id": "MIM:609033",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/609033",
            "name": "Retinopathy-sensory neuropathy syndrome",
            "description": "Retinopathy-sensory neuropathy syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061157"
    ],
    "unlinked_id_list": []
}