{
    "disease_id": "DOID:0110405",
    "recommended_name": {
        "id": "DOID:0110405",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110405",
        "name": "retinitis pigmentosa 36",
        "description": "A retinitis pigmentosa that has_material_basis_in mutation in the PRCD gene on chromosome 17q25."
    },
    "synonyms": [
        {
            "id": "DOID:0110405",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110405",
            "name": "RP36",
            "description": ""
        },
        {
            "id": "MONDO:0012523",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012523",
            "name": "retinitis pigmentosa 36",
            "description": "Any retinitis pigmentosa in which the cause of the disease is a mutation in the PRCD gene."
        },
        {
            "id": "MONDO:0012523",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012523",
            "name": "PRCD retinitis pigmentosa",
            "description": ""
        },
        {
            "id": "MONDO:0012523",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012523",
            "name": "RP36",
            "description": ""
        },
        {
            "id": "MONDO:0012523",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012523",
            "name": "retinitis pigmentosa 36",
            "description": ""
        },
        {
            "id": "MONDO:0012523",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012523",
            "name": "retinitis pigmentosa caused by mutation in PRCD",
            "description": ""
        },
        {
            "id": "MONDO:0012523",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012523",
            "name": "retinitis pigmentosa type 36",
            "description": ""
        },
        {
            "id": "MONDO:0012523",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012523",
            "name": "RP 36",
            "description": ""
        },
        {
            "id": "MIM:610599",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/610599",
            "name": "Retinitis pigmentosa 36",
            "description": "Retinitis pigmentosa 36"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110405"
    ],
    "unlinked_id_list": [],
    "crossref": [
        {
            "id": "DOID:0110405",
            "database": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110405",
            "categories": []
        },
        {
            "id": "MONDO:0012523",
            "database": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012523",
            "categories": []
        },
        {
            "id": "MIM:610599",
            "database": "MIM",
            "url": "https://www.omim.org/entry/610599",
            "categories": []
        }
    ],
    "proteins": [
        {
            "uniprot_canonical_ac": "Q00LT2-1",
            "uniprot_ac": "Q00LT2",
            "uniprot_id": "PRCD_MOUSE",
            "refseq_ac": "NP_001156790",
            "glycoprotein": "no",
            "species": [
                {
                    "name": "Mus musculus",
                    "taxid": 10090,
                    "common_name": "Mouse",
                    "glygen_name": "Mouse",
                    "reference_species": "Mus musculus [10090]"
                }
            ],
            "protein_names": [
                {
                    "name": "Photoreceptor disk component PRCD",
                    "type": "recommended"
                },
                {
                    "name": "Progressive rod-cone degeneration protein homolog",
                    "type": "synonym"
                },
                {
                    "name": "photoreceptor disk component PRCD",
                    "type": "synonym"
                },
                {
                    "name": "progressive rod cone degeneration protein",
                    "type": "synonym"
                },
                {
                    "name": "progressive rod-cone degeneration protein homolog",
                    "type": "synonym"
                }
            ],
            "gene_names": [
                {
                    "name": "Prcd",
                    "type": "recommended"
                },
                {
                    "name": "Gm11744",
                    "type": "synonym"
                },
                {
                    "name": "Prcd",
                    "type": "synonym"
                }
            ],
            "record_id": "Q00LT2-1",
            "evidence": [
                {
                    "id": "0110405",
                    "database": "AGR",
                    "url": "https://www.alliancegenome.org/disease/DOID:0110405"
                }
            ]
        },
        {
            "uniprot_canonical_ac": "Q00LT1-1",
            "uniprot_ac": "Q00LT1",
            "uniprot_id": "PRCD_HUMAN",
            "refseq_ac": "NP_001071088",
            "glycoprotein": "no",
            "species": [
                {
                    "name": "Homo sapiens",
                    "taxid": 9606,
                    "common_name": "Human",
                    "glygen_name": "Human",
                    "reference_species": "Homo sapiens [9606]"
                }
            ],
            "protein_names": [
                {
                    "name": "Photoreceptor disk component PRCD",
                    "type": "recommended"
                },
                {
                    "name": "Progressive rod-cone degeneration protein",
                    "type": "synonym"
                },
                {
                    "name": "photoreceptor disk component PRCD",
                    "type": "synonym"
                },
                {
                    "name": "progressive rod-cone degeneration protein",
                    "type": "synonym"
                }
            ],
            "gene_names": [
                {
                    "name": "PRCD",
                    "type": "recommended"
                },
                {
                    "name": "PRCD",
                    "type": "synonym"
                },
                {
                    "name": "RP36",
                    "type": "synonym"
                }
            ],
            "record_id": "Q00LT1-1",
            "evidence": [
                {
                    "id": "610599",
                    "database": "MIM",
                    "url": "https://www.omim.org/entry/610599"
                },
                {
                    "id": "0110405",
                    "database": "AGR",
                    "url": "https://www.alliancegenome.org/disease/DOID:0110405"
                }
            ]
        },
        {
            "uniprot_canonical_ac": "A0ABK0M2A6-1",
            "uniprot_ac": "A0ABK0M2A6",
            "uniprot_id": "A0ABK0M2A6_RAT",
            "refseq_ac": "XP_017453237",
            "glycoprotein": "no",
            "species": [
                {
                    "name": "Rattus norvegicus",
                    "taxid": 10116,
                    "common_name": "Rat",
                    "glygen_name": "Rat",
                    "reference_species": "Rattus norvegicus [10116]"
                }
            ],
            "protein_names": [
                {
                    "name": "Photoreceptor disc component",
                    "type": "synonym"
                },
                {
                    "name": "photoreceptor disk component PRCD isoform X1",
                    "type": "synonym"
                }
            ],
            "gene_names": [
                {
                    "name": "Prcd",
                    "type": "recommended"
                },
                {
                    "name": "Prcd",
                    "type": "synonym"
                }
            ],
            "record_id": "A0ABK0M2A6-1",
            "evidence": [
                {
                    "id": "0110405",
                    "database": "AGR",
                    "url": "https://www.alliancegenome.org/disease/DOID:0110405"
                }
            ]
        }
    ],
    "glycans": [],
    "biomarkers": [],
    "association_flag": "1000",
    "record_id": "doid.0110405"
}