{
    "disease_id": "DOID:0110791",
    "recommended_name": {
        "id": "DOID:0110791",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110791",
        "name": "hereditary spastic paraplegia 3A",
        "description": "A hereditary spastic paraplegia that is characterized by lower limb weakness and spasticity that is generally non-progressive or extremely slow and has_material_basis_in mutation in the ATL1 gene on chromosome 14q22."
    },
    "synonyms": [
        {
            "id": "DOID:0110791",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110791",
            "name": "FSP1",
            "description": ""
        },
        {
            "id": "DOID:0110791",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110791",
            "name": "SPG3A",
            "description": ""
        },
        {
            "id": "DOID:0110791",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110791",
            "name": "autosomal dominant familial spastic paraplegia 1",
            "description": ""
        },
        {
            "id": "DOID:0110791",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110791",
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            "description": ""
        },
        {
            "id": "DOID:0110791",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110791",
            "name": "autosomal dominant spastic paraplegia type 3",
            "description": ""
        },
        {
            "id": "DOID:0110791",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110791",
            "name": "strumpell disease",
            "description": ""
        },
        {
            "id": "MONDO:0008437",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008437",
            "name": "hereditary spastic paraplegia 3A",
            "description": "Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the ATL1 gene."
        },
        {
            "id": "MONDO:0008437",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008437",
            "name": "ATL1 hereditary spastic paraplegia",
            "description": ""
        },
        {
            "id": "MONDO:0008437",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008437",
            "name": "FSP1",
            "description": ""
        },
        {
            "id": "MONDO:0008437",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008437",
            "name": "SPG3A",
            "description": ""
        },
        {
            "id": "MONDO:0008437",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008437",
            "name": "Strmpell disease",
            "description": ""
        },
        {
            "id": "MONDO:0008437",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008437",
            "name": "autosomal dominant spastic paraplegia type 3",
            "description": ""
        },
        {
            "id": "MONDO:0008437",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008437",
            "name": "hereditary spastic paraplegia caused by mutation in ATL1",
            "description": ""
        },
        {
            "id": "MONDO:0008437",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008437",
            "name": "hereditary spastic paraplegia type 3A",
            "description": ""
        },
        {
            "id": "MONDO:0008437",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008437",
            "name": "spastic Paraplegia 3A",
            "description": ""
        },
        {
            "id": "MONDO:0008437",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008437",
            "name": "spastic paraplegia 3a, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008437",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008437",
            "name": "strumpell disease",
            "description": ""
        },
        {
            "id": "MONDO:0008437",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008437",
            "name": "spastic paraplegia 3",
            "description": ""
        },
        {
            "id": "MONDO:0008437",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008437",
            "name": "spastic paraplegia 3, autosomal dominant",
            "description": ""
        },
        {
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            "resource": "MIM",
            "url": "https://www.omim.org/entry/182600",
            "name": "Spastic paraplegia 3, autosomal dominant",
            "description": "Spastic paraplegia 3, autosomal dominant"
        }
    ],
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    ],
    "unlinked_id_list": [],
    "crossref": [
        {
            "id": "DOID:0110791",
            "database": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110791",
            "categories": []
        },
        {
            "id": "MONDO:0008437",
            "database": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008437",
            "categories": []
        },
        {
            "id": "MIM:182600",
            "database": "MIM",
            "url": "https://www.omim.org/entry/182600",
            "categories": []
        }
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                {
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                }
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        },
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                    "reference_species": "Mus musculus [10090]"
                }
            ],
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                    "name": "Atlastin-1",
                    "type": "recommended"
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                {
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                    "name": "Atl1",
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                    "name": "4930435M24Rik",
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                    "type": "synonym"
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                {
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                    "name": "Spg3a",
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                    "name": "Spg3",
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            ],
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            ],
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                    "name": "5730596K20Rik",
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                {
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                {
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                    "name": "Homo sapiens",
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                {
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                {
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                    "id": "0110791",
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                    "name": "Drosophila melanogaster",
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                    "reference_species": "Drosophila melanogaster [7227]"
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                    "name": "D-atlastin",
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                {
                    "name": "Atl",
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                    "name": "CG6668",
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                    "name": "DATL",
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                {
                    "name": "Dmel\\CG6668",
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                {
                    "name": "Dmel_CG6668",
                    "type": "synonym"
                },
                {
                    "name": "atl",
                    "type": "synonym"
                },
                {
                    "name": "dAtl",
                    "type": "synonym"
                }
            ],
            "record_id": "Q9VC57-1",
            "evidence": [
                {
                    "id": "0110791",
                    "database": "AGR",
                    "url": "https://www.alliancegenome.org/disease/DOID:0110791"
                }
            ]
        },
        {
            "uniprot_canonical_ac": "Q6DD88-1",
            "uniprot_ac": "Q6DD88",
            "uniprot_id": "ATLA3_HUMAN",
            "refseq_ac": "NP_001276977",
            "glycoprotein": "yes",
            "species": [
                {
                    "name": "Homo sapiens",
                    "taxid": 9606,
                    "common_name": "Human",
                    "glygen_name": "Human",
                    "reference_species": "Homo sapiens [9606]"
                }
            ],
            "protein_names": [
                {
                    "name": "Atlastin-3",
                    "type": "recommended"
                },
                {
                    "name": "3.6.5.-",
                    "type": "synonym"
                },
                {
                    "name": "AT3",
                    "type": "synonym"
                },
                {
                    "name": "ATL-3",
                    "type": "synonym"
                },
                {
                    "name": "atlastin-3 isoform 2",
                    "type": "synonym"
                },
                {
                    "name": "atlastin-3",
                    "type": "synonym"
                }
            ],
            "gene_names": [
                {
                    "name": "ATL3",
                    "type": "recommended"
                },
                {
                    "name": "AT3",
                    "type": "synonym"
                },
                {
                    "name": "ATL-3",
                    "type": "synonym"
                },
                {
                    "name": "ATL3",
                    "type": "synonym"
                },
                {
                    "name": "HSN1F",
                    "type": "synonym"
                }
            ],
            "record_id": "Q6DD88-1",
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                {
                    "id": "0110791",
                    "database": "AGR",
                    "url": "https://www.alliancegenome.org/disease/DOID:0110791"
                }
            ]
        },
        {
            "uniprot_canonical_ac": "Q8NHH9-1",
            "uniprot_ac": "Q8NHH9",
            "uniprot_id": "ATLA2_HUMAN",
            "refseq_ac": "NP_001129145",
            "glycoprotein": "yes",
            "species": [
                {
                    "name": "Homo sapiens",
                    "taxid": 9606,
                    "common_name": "Human",
                    "glygen_name": "Human",
                    "reference_species": "Homo sapiens [9606]"
                }
            ],
            "protein_names": [
                {
                    "name": "Atlastin-2",
                    "type": "recommended"
                },
                {
                    "name": "3.6.5.-",
                    "type": "synonym"
                },
                {
                    "name": "ADP-ribosylation factor-like protein 6-interacting protein 2",
                    "type": "synonym"
                },
                {
                    "name": "ARL-6-interacting protein 2",
                    "type": "synonym"
                },
                {
                    "name": "ATL-2",
                    "type": "synonym"
                },
                {
                    "name": "atlastin-2 isoform 2",
                    "type": "synonym"
                }
            ],
            "gene_names": [
                {
                    "name": "ATL2",
                    "type": "recommended"
                },
                {
                    "name": "ARL3IP2",
                    "type": "synonym"
                },
                {
                    "name": "ARL6IP2",
                    "type": "synonym"
                },
                {
                    "name": "ATL-2",
                    "type": "synonym"
                },
                {
                    "name": "ATL2",
                    "type": "synonym"
                },
                {
                    "name": "aip-2",
                    "type": "synonym"
                },
                {
                    "name": "atlastin2",
                    "type": "synonym"
                }
            ],
            "record_id": "Q8NHH9-1",
            "evidence": [
                {
                    "id": "0110791",
                    "database": "AGR",
                    "url": "https://www.alliancegenome.org/disease/DOID:0110791"
                }
            ]
        }
    ],
    "glycans": [],
    "biomarkers": [],
    "association_flag": "1000",
    "record_id": "doid.0110791"
}