{
    "disease_id": "DOID:0061296",
    "recommended_name": {
        "id": "DOID:0061296",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061296",
        "name": "Meckel syndrome 11",
        "description": "A Meckel syndrome that has_material_basis_in homozygous mutation in the TMEM231 gene on chromosome 16q23."
    },
    "synonyms": [
        {
            "id": "MONDO:0014164",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014164",
            "name": "Meckel syndrome, type 11",
            "description": "Any Meckel syndrome in which the cause of the disease is a mutation in the TMEM231 gene."
        },
        {
            "id": "MONDO:0014164",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014164",
            "name": "Meckel syndrome caused by mutation in TMEM231",
            "description": ""
        },
        {
            "id": "MONDO:0014164",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014164",
            "name": "Meckel syndrome, type 11",
            "description": ""
        },
        {
            "id": "MONDO:0014164",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014164",
            "name": "TMEM231 Meckel syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014164",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014164",
            "name": "meckel syndrome 11",
            "description": ""
        },
        {
            "id": "MONDO:0014164",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014164",
            "name": "MKS11",
            "description": ""
        },
        {
            "id": "MIM:615397",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615397",
            "name": "Meckel syndrome 11",
            "description": "Meckel syndrome 11"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061296"
    ],
    "unlinked_id_list": [],
    "crossref": [
        {
            "id": "DOID:0061296",
            "database": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061296",
            "categories": []
        },
        {
            "id": "MONDO:0014164",
            "database": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014164",
            "categories": []
        },
        {
            "id": "MIM:615397",
            "database": "MIM",
            "url": "https://www.omim.org/entry/615397",
            "categories": []
        }
    ],
    "proteins": [
        {
            "uniprot_canonical_ac": "Q9H6L2-1",
            "uniprot_ac": "Q9H6L2",
            "uniprot_id": "TM231_HUMAN",
            "refseq_ac": "NP_001070884",
            "glycoprotein": "yes",
            "species": [
                {
                    "name": "Homo sapiens",
                    "taxid": 9606,
                    "common_name": "Human",
                    "glygen_name": "Human",
                    "reference_species": "Homo sapiens [9606]"
                }
            ],
            "protein_names": [
                {
                    "name": "Transmembrane protein 231",
                    "type": "recommended"
                },
                {
                    "name": "transmembrane protein 231 isoform 1",
                    "type": "synonym"
                }
            ],
            "gene_names": [
                {
                    "name": "TMEM231",
                    "type": "recommended"
                },
                {
                    "name": "ALYE870",
                    "type": "synonym"
                },
                {
                    "name": "JBTS20",
                    "type": "synonym"
                },
                {
                    "name": "MKS11",
                    "type": "synonym"
                },
                {
                    "name": "PRO1886",
                    "type": "synonym"
                },
                {
                    "name": "TMEM231",
                    "type": "synonym"
                }
            ],
            "record_id": "Q9H6L2-1",
            "evidence": [
                {
                    "id": "615397",
                    "database": "MIM",
                    "url": "https://www.omim.org/entry/615397"
                }
            ]
        }
    ],
    "glycans": [],
    "biomarkers": [],
    "association_flag": "1000",
    "record_id": "doid.0061296"
}