{
    "disease_id": "DOID:0061252",
    "recommended_name": {
        "id": "DOID:0061252",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061252",
        "name": "neurodevelopmental disorder with hypotonia, epilepsy, and absent speech",
        "description": "An autosomal recessive intellectual developmental disorder characterized by infantile hypotonia, profoundly impaired motor and cognitive development, absent speech, and early-onset seizures that has_material_basis_in homozygous or compound heterozygous mutation in the UNC13A gene on chromosome 19p13."
    },
    "synonyms": [
        {
            "id": "MONDO:0980940",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0980940",
            "name": "neurodevelopmental disorder with hypotonia, epilepsy, and absent speech",
            "description": ""
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061252"
    ],
    "unlinked_id_list": [],
    "crossref": [
        {
            "id": "DOID:0061252",
            "database": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061252",
            "categories": []
        },
        {
            "id": "MONDO:0980940",
            "database": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0980940",
            "categories": []
        }
    ],
    "proteins": [
        {
            "uniprot_canonical_ac": "Q9UPW8-1",
            "uniprot_ac": "Q9UPW8",
            "uniprot_id": "UN13A_HUMAN",
            "refseq_ac": "NP_001073890",
            "glycoprotein": "yes",
            "species": [
                {
                    "name": "Homo sapiens",
                    "taxid": 9606,
                    "common_name": "Human",
                    "glygen_name": "Human",
                    "reference_species": "Homo sapiens [9606]"
                }
            ],
            "protein_names": [
                {
                    "name": "Protein unc-13 homolog A",
                    "type": "recommended"
                },
                {
                    "name": "Munc13-1",
                    "type": "synonym"
                },
                {
                    "name": "protein unc-13 homolog A isoform 1",
                    "type": "synonym"
                },
                {
                    "name": "protein unc-13 homolog A",
                    "type": "synonym"
                }
            ],
            "gene_names": [
                {
                    "name": "UNC13A",
                    "type": "recommended"
                },
                {
                    "name": "IDDSF",
                    "type": "synonym"
                },
                {
                    "name": "KIAA1032",
                    "type": "synonym"
                },
                {
                    "name": "Munc13-1",
                    "type": "synonym"
                },
                {
                    "name": "NEDHES",
                    "type": "synonym"
                },
                {
                    "name": "NEDSMS",
                    "type": "synonym"
                },
                {
                    "name": "UNC13A",
                    "type": "synonym"
                }
            ],
            "record_id": "Q9UPW8-1",
            "evidence": [
                {
                    "id": "621455",
                    "database": "MIM",
                    "url": "https://www.omim.org/entry/621455"
                }
            ]
        }
    ],
    "glycans": [],
    "biomarkers": [],
    "association_flag": "1000",
    "record_id": "doid.0061252"
}