{
    "disease_id": "DOID:0110735",
    "recommended_name": {
        "id": "DOID:0110735",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110735",
        "name": "neurodegeneration with brain iron accumulation 2a",
        "description": "A neurodegeneration with brain iron accumulation that has_material_basis_in autosomal recessive inheritance of mutation in the PLA2G6 gene on chromosome 22q13.1 and is characterized by onset in the first 2 years of life."
    },
    "synonyms": [
        {
            "id": "DOID:0110735",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110735",
            "name": "INAD1",
            "description": ""
        },
        {
            "id": "DOID:0110735",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110735",
            "name": "Infantile Neuroaxonal Dystrophy 1",
            "description": ""
        },
        {
            "id": "DOID:0110735",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110735",
            "name": "NBIA2a",
            "description": ""
        },
        {
            "id": "DOID:0110735",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110735",
            "name": "Neurodegeneration, Pla2g6-Associated",
            "description": ""
        },
        {
            "id": "DOID:0110735",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110735",
            "name": "Seitelberger Disease",
            "description": ""
        },
        {
            "id": "MONDO:0024457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024457",
            "name": "neurodegeneration with brain iron accumulation 2A",
            "description": ""
        },
        {
            "id": "MONDO:0024457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024457",
            "name": "Seitelberger disease",
            "description": ""
        },
        {
            "id": "MONDO:0024457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024457",
            "name": "INAD",
            "description": ""
        },
        {
            "id": "MONDO:0024457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024457",
            "name": "NBIA2A",
            "description": ""
        },
        {
            "id": "MONDO:0024457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024457",
            "name": "NBIA2a",
            "description": ""
        },
        {
            "id": "MONDO:0024457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024457",
            "name": "PLAN",
            "description": ""
        },
        {
            "id": "MONDO:0024457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024457",
            "name": "inaD",
            "description": ""
        },
        {
            "id": "MONDO:0024457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024457",
            "name": "infantile neuroaxonal dystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0024457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024457",
            "name": "neurodegeneration with brain iron accumulation 2A",
            "description": ""
        },
        {
            "id": "MONDO:0024457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024457",
            "name": "neurodegeneration with brain iron accumulation type 2A",
            "description": ""
        },
        {
            "id": "MONDO:0024457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024457",
            "name": "neurodegeneration with brain iron accumulation type 2a",
            "description": ""
        },
        {
            "id": "MONDO:0024457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024457",
            "name": "neurodegeneration, PLA2G6-associated",
            "description": ""
        },
        {
            "id": "MONDO:0024457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024457",
            "name": "neurodegeneration, Pla2G6-associated",
            "description": ""
        },
        {
            "id": "MONDO:0024457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024457",
            "name": "neurodegeneration, Pla2g6-associated",
            "description": ""
        },
        {
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            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024457",
            "name": "phospholipase A2-associated neurodegeneration",
            "description": ""
        },
        {
            "id": "MONDO:0024457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024457",
            "name": "Hunter Carpenter Macdonald syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0024457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024457",
            "name": "Hunter-Carpenter-McDonald syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0024457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024457",
            "name": "INAD1",
            "description": ""
        },
        {
            "id": "MONDO:0024457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024457",
            "name": "KARAK syndrome, included",
            "description": ""
        },
        {
            "id": "MONDO:0024457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024457",
            "name": "infantile neuroaxonal dystrophy/atypical neuroaxonal dystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0024457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024457",
            "name": "neuroaxonal dystrophy presenting with neonatal dysmorphic features, early onset of peripheral gangrene",
            "description": ""
        },
        {
            "id": "MIM:256600",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/256600",
            "name": "Neurodegeneration with brain iron accumulation 2A",
            "description": "Neurodegeneration with brain iron accumulation 2A"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110735"
    ],
    "unlinked_id_list": []
}