{
    "disease_id": "DOID:0110462",
    "recommended_name": {
        "id": "DOID:0110462",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110462",
        "name": "autosomal recessive nonsyndromic deafness 101",
        "description": "An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the GRXCR2 gene on chromosome 5q32."
    },
    "synonyms": [
        {
            "id": "DOID:0110462",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110462",
            "name": "DFNB101",
            "description": ""
        },
        {
            "id": "DOID:0110462",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110462",
            "name": "autosomal recessive deafness 101",
            "description": ""
        },
        {
            "id": "MONDO:0014363",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014363",
            "name": "autosomal recessive nonsyndromic hearing loss 101",
            "description": "Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the GRXCR2 gene."
        },
        {
            "id": "MONDO:0014363",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014363",
            "name": "DFNB101",
            "description": ""
        },
        {
            "id": "MONDO:0014363",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014363",
            "name": "GRXCR2 autosomal recessive nonsyndromic deafness",
            "description": ""
        },
        {
            "id": "MONDO:0014363",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014363",
            "name": "autosomal recessive deafness 101",
            "description": ""
        },
        {
            "id": "MONDO:0014363",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014363",
            "name": "autosomal recessive nonsyndromic deafness 101",
            "description": ""
        },
        {
            "id": "MONDO:0014363",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014363",
            "name": "autosomal recessive nonsyndromic deafness caused by mutation in GRXCR2",
            "description": ""
        },
        {
            "id": "MONDO:0014363",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014363",
            "name": "autosomal recessive nonsyndromic deafness type 101",
            "description": ""
        },
        {
            "id": "MONDO:0014363",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014363",
            "name": "deafness, autosomal recessive 101",
            "description": ""
        },
        {
            "id": "MONDO:0014363",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014363",
            "name": "deafness, autosomal recessive type 101",
            "description": ""
        },
        {
            "id": "MIM:615837",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615837",
            "name": "Deafness, autosomal recessive, 101",
            "description": "Deafness, autosomal recessive, 101"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110462"
    ],
    "unlinked_id_list": [],
    "crossref": [
        {
            "id": "DOID:0110462",
            "database": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110462",
            "categories": []
        },
        {
            "id": "MONDO:0014363",
            "database": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014363",
            "categories": []
        },
        {
            "id": "MIM:615837",
            "database": "MIM",
            "url": "https://www.omim.org/entry/615837",
            "categories": []
        }
    ],
    "proteins": [
        {
            "uniprot_canonical_ac": "Q3TYR5-1",
            "uniprot_ac": "Q3TYR5",
            "uniprot_id": "GRCR2_MOUSE",
            "refseq_ac": "NP_001028598",
            "glycoprotein": "no",
            "species": [
                {
                    "name": "Mus musculus",
                    "taxid": 10090,
                    "common_name": "Mouse",
                    "glygen_name": "Mouse",
                    "reference_species": "Mus musculus [10090]"
                }
            ],
            "protein_names": [
                {
                    "name": "Glutaredoxin domain-containing cysteine-rich protein 2",
                    "type": "recommended"
                },
                {
                    "name": "GRXCR1-like protein",
                    "type": "synonym"
                },
                {
                    "name": "Glutaredoxin domain-containing cysteine-rich protein 1-like protein",
                    "type": "synonym"
                },
                {
                    "name": "glutaredoxin domain-containing cysteine-rich protein 1-like protein",
                    "type": "synonym"
                },
                {
                    "name": "glutaredoxin domain-containing cysteine-rich protein 2",
                    "type": "synonym"
                }
            ],
            "gene_names": [
                {
                    "name": "Grxcr2",
                    "type": "recommended"
                },
                {
                    "name": "Gm851",
                    "type": "synonym"
                },
                {
                    "name": "Grxcr2",
                    "type": "synonym"
                }
            ],
            "record_id": "Q3TYR5-1",
            "evidence": [
                {
                    "id": "0110462",
                    "database": "AGR",
                    "url": "https://www.alliancegenome.org/disease/DOID:0110462"
                }
            ]
        },
        {
            "uniprot_canonical_ac": "A6NFK2-1",
            "uniprot_ac": "A6NFK2",
            "uniprot_id": "GRCR2_HUMAN",
            "refseq_ac": "NP_001073985",
            "glycoprotein": "no",
            "species": [
                {
                    "name": "Homo sapiens",
                    "taxid": 9606,
                    "common_name": "Human",
                    "glygen_name": "Human",
                    "reference_species": "Homo sapiens [9606]"
                }
            ],
            "protein_names": [
                {
                    "name": "Glutaredoxin domain-containing cysteine-rich protein 2",
                    "type": "recommended"
                },
                {
                    "name": "GRXCR1-like protein",
                    "type": "synonym"
                },
                {
                    "name": "Glutaredoxin domain-containing cysteine-rich protein 1-like protein",
                    "type": "synonym"
                },
                {
                    "name": "glutaredoxin domain-containing cysteine-rich protein 1-like protein",
                    "type": "synonym"
                },
                {
                    "name": "glutaredoxin domain-containing cysteine-rich protein 2",
                    "type": "synonym"
                },
                {
                    "name": "glutaredoxin, cysteine rich 2",
                    "type": "synonym"
                }
            ],
            "gene_names": [
                {
                    "name": "GRXCR2",
                    "type": "recommended"
                },
                {
                    "name": "DFNB101",
                    "type": "synonym"
                },
                {
                    "name": "GRXCR2",
                    "type": "synonym"
                }
            ],
            "record_id": "A6NFK2-1",
            "evidence": [
                {
                    "id": "615837",
                    "database": "MIM",
                    "url": "https://www.omim.org/entry/615837"
                },
                {
                    "id": "0110462",
                    "database": "AGR",
                    "url": "https://www.alliancegenome.org/disease/DOID:0110462"
                }
            ]
        },
        {
            "uniprot_canonical_ac": "D4ABJ8-1",
            "uniprot_ac": "D4ABJ8",
            "uniprot_id": "D4ABJ8_RAT",
            "refseq_ac": "",
            "glycoprotein": "no",
            "species": [
                {
                    "name": "Rattus norvegicus",
                    "taxid": 10116,
                    "common_name": "Rat",
                    "glygen_name": "Rat",
                    "reference_species": "Rattus norvegicus [10116]"
                }
            ],
            "protein_names": [
                {
                    "name": "Glutaredoxin and cysteine rich domain containing 2",
                    "type": "synonym"
                }
            ],
            "gene_names": [
                {
                    "name": "Grxcr2",
                    "type": "recommended"
                }
            ],
            "record_id": "D4ABJ8-1",
            "evidence": [
                {
                    "id": "0110462",
                    "database": "AGR",
                    "url": "https://www.alliancegenome.org/disease/DOID:0110462"
                }
            ]
        }
    ],
    "glycans": [],
    "biomarkers": [],
    "association_flag": "1000",
    "record_id": "doid.0110462"
}