{
    "disease_id": "DOID:0070357",
    "recommended_name": {
        "id": "DOID:0070357",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070357",
        "name": "nephrotic syndrome type 20",
        "description": "A familial nephrotic syndrome that has_material_basis_in X-linked renal disorder characterized by onset of steroid-resistant nephrotic syndrome and proteinuria in the first years of life in affected males."
    },
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            "id": "MONDO:0026726",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0026726",
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            "description": ""
        },
        {
            "id": "MONDO:0026726",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0026726",
            "name": "NPHS20",
            "description": ""
        },
        {
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            "resource": "MIM",
            "url": "https://www.omim.org/entry/301028",
            "name": "Nephrotic syndrome 20",
            "description": "Nephrotic syndrome 20"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070357"
    ],
    "unlinked_id_list": [],
    "crossref": [
        {
            "id": "DOID:0070357",
            "database": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070357",
            "categories": []
        },
        {
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            "url": "https://monarchinitiative.org/disease/MONDO:0026726",
            "categories": []
        },
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            "url": "https://www.omim.org/entry/301028",
            "categories": []
        }
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                }
            ],
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                    "type": "synonym"
                },
                {
                    "name": "VRP",
                    "type": "synonym"
                }
            ],
            "record_id": "O95759-1",
            "evidence": [
                {
                    "id": "0070357",
                    "database": "AGR",
                    "url": "https://www.alliancegenome.org/disease/DOID:0070357"
                }
            ]
        },
        {
            "uniprot_canonical_ac": "Q66K14-1",
            "uniprot_ac": "Q66K14",
            "uniprot_id": "TBC9B_HUMAN",
            "refseq_ac": "NP_055858",
            "glycoprotein": "yes",
            "species": [
                {
                    "name": "Homo sapiens",
                    "taxid": 9606,
                    "common_name": "Human",
                    "glygen_name": "Human",
                    "reference_species": "Homo sapiens [9606]"
                }
            ],
            "protein_names": [
                {
                    "name": "TBC1 domain family member 9B",
                    "type": "recommended"
                },
                {
                    "name": "TBC1 domain family member 9B isoform b",
                    "type": "synonym"
                },
                {
                    "name": "TBC1 domain family, member 9B (with GRAM domain)",
                    "type": "synonym"
                }
            ],
            "gene_names": [
                {
                    "name": "TBC1D9B",
                    "type": "recommended"
                },
                {
                    "name": "GRAMD9B",
                    "type": "synonym"
                },
                {
                    "name": "KIAA0676",
                    "type": "synonym"
                },
                {
                    "name": "TBC1D9B",
                    "type": "synonym"
                }
            ],
            "record_id": "Q66K14-1",
            "evidence": [
                {
                    "id": "0070357",
                    "database": "AGR",
                    "url": "https://www.alliancegenome.org/disease/DOID:0070357"
                }
            ]
        }
    ],
    "glycans": [],
    "biomarkers": [],
    "association_flag": "1000",
    "record_id": "doid.0070357"
}