{
    "disease_id": "DOID:0060810",
    "recommended_name": {
        "id": "DOID:0060810",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060810",
        "name": "syndromic X-linked intellectual disability type 10",
        "description": "A syndromic X-linked intellectual disability characterized by mild intellectual deficit associated with choreoathetosis and abnormal behaviour that has_material_basis_in mutation in the HSD17B10 gene on chromosome Xp11.22."
    },
    "synonyms": [
        {
            "id": "DOID:0060810",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060810",
            "name": "HSD10 deficiency, atypical type",
            "description": ""
        },
        {
            "id": "DOID:0060810",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060810",
            "name": "HSD10 disease, atypical type",
            "description": ""
        },
        {
            "id": "DOID:0060810",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060810",
            "name": "MRXS10",
            "description": ""
        },
        {
            "id": "DOID:0060810",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060810",
            "name": "X-linked intellectual disability-choreoathetosis-abnormal behavior syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060810",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060810",
            "name": "mental retardation, X-linked syndromic 10",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "HSD10 mitochondrial disease",
            "description": "A rare, life-threatening neurometabolic disease characterized by a progressive neurodegenerative course, epilepsy, retinopathy and progressive cardiomyopathy."
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "17-beta-hydroxysteroid dehydrogenase 10 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "17-beta-hydroxysteroid dehydrogenase X deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "2-methyl-3-hydroxybutyric aciduria",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "3-hydroxyacyl-CoA dehydrogenase 2 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "HSD10 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "HSD10 mitochondrial disease",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "HSD10 mitochondrial disease, X-linked dominant",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "HSD10MD",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "HSD17B10 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "MHBD deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "MRXS10",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "chorioathetosis with mental retardation and abnormal behavior",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "chorioathetosis with mental retardation and abnormal behaviour",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "mental retardation with chorioathetosis and abnormal behavior",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "mental retardation with chorioathetosis and abnormal behaviour",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "mental retardation, X-linked, syndromic 10",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "mental retardation, X-linked, syndromic type 10",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "HSD10 deficiency, atypical type",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "X-linked intellectual disability-choreoathetosis-abnormal behavior syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "X-linked intellectual disability-choreoathetosis-abnormal behaviour syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "syndromic X-linked intellectual disability type 10",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "17 beta-hydroxysteroid dehydrogenase type 10 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "2M3HBA",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "3-hydroxy-2-methylbutyryl-CoA dehydrogenase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "3H2MBD deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "hydroxyacyl-CoA dehydrogenase II deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "HSD10 mitochondrial disease",
            "description": "A rare, life-threatening neurometabolic disease characterized by a progressive neurodegenerative course, epilepsy, retinopathy and progressive cardiomyopathy."
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "17-beta-hydroxysteroid dehydrogenase 10 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "17-beta-hydroxysteroid dehydrogenase X deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "2-methyl-3-hydroxybutyric aciduria",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "3-hydroxyacyl-CoA dehydrogenase 2 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "HSD10 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "HSD10 mitochondrial disease",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "HSD10 mitochondrial disease, X-linked dominant",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "HSD10MD",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "HSD17B10 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "MHBD deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "MRXS10",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "chorioathetosis with mental retardation and abnormal behavior",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "chorioathetosis with mental retardation and abnormal behaviour",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "mental retardation with chorioathetosis and abnormal behavior",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "mental retardation with chorioathetosis and abnormal behaviour",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "mental retardation, X-linked, syndromic 10",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "mental retardation, X-linked, syndromic type 10",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "HSD10 deficiency, atypical type",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "X-linked intellectual disability-choreoathetosis-abnormal behavior syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "X-linked intellectual disability-choreoathetosis-abnormal behaviour syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "syndromic X-linked intellectual disability type 10",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "17 beta-hydroxysteroid dehydrogenase type 10 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "2M3HBA",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "3-hydroxy-2-methylbutyryl-CoA dehydrogenase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "3H2MBD deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "name": "hydroxyacyl-CoA dehydrogenase II deficiency",
            "description": ""
        },
        {
            "id": "MIM:300438",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300438",
            "name": "HSD10 mitochondrial disease",
            "description": "HSD10 mitochondrial disease"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060810"
    ],
    "unlinked_id_list": [],
    "crossref": [
        {
            "id": "DOID:0060810",
            "database": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060810",
            "categories": []
        },
        {
            "id": "MONDO:0010327",
            "database": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010327",
            "categories": []
        },
        {
            "id": "MIM:300438",
            "database": "MIM",
            "url": "https://www.omim.org/entry/300438",
            "categories": []
        }
    ],
    "proteins": [
        {
            "uniprot_canonical_ac": "O08756-1",
            "uniprot_ac": "O08756",
            "uniprot_id": "HCD2_MOUSE",
            "refseq_ac": "",
            "glycoprotein": "yes",
            "species": [
                {
                    "name": "Mus musculus",
                    "taxid": 10090,
                    "common_name": "Mouse",
                    "glygen_name": "Mouse",
                    "reference_species": "Mus musculus [10090]"
                }
            ],
            "protein_names": [
                {
                    "name": "3-hydroxyacyl-CoA dehydrogenase type-2",
                    "type": "recommended"
                },
                {
                    "name": "1.1.1.159",
                    "type": "synonym"
                },
                {
                    "name": "1.1.1.178",
                    "type": "synonym"
                },
                {
                    "name": "1.1.1.239",
                    "type": "synonym"
                },
                {
                    "name": "1.1.1.35",
                    "type": "synonym"
                },
                {
                    "name": "1.1.1.53",
                    "type": "synonym"
                },
                {
                    "name": "1.1.1.62",
                    "type": "synonym"
                },
                {
                    "name": "17-beta-estradiol 17-dehydrogenase",
                    "type": "synonym"
                },
                {
                    "name": "2-methyl-3-hydroxybutyryl-CoA dehydrogenase",
                    "type": "synonym"
                },
                {
                    "name": "3-alpha-(17-beta)-hydroxysteroid dehydrogenase (NAD(+))",
                    "type": "synonym"
                },
                {
                    "name": "3-hydroxy-2-methylbutyryl-CoA dehydrogenase",
                    "type": "synonym"
                },
                {
                    "name": "3-hydroxyacyl-CoA dehydrogenase type II",
                    "type": "synonym"
                },
                {
                    "name": "3alpha(or 20beta)-hydroxysteroid dehydrogenase",
                    "type": "synonym"
                },
                {
                    "name": "7-alpha-hydroxysteroid dehydrogenase",
                    "type": "synonym"
                },
                {
                    "name": "Endoplasmic reticulum-associated amyloid beta-peptide-binding protein",
                    "type": "synonym"
                },
                {
                    "name": "MHBD",
                    "type": "synonym"
                },
                {
                    "name": "Mitochondrial RNase P protein 2",
                    "type": "synonym"
                },
                {
                    "name": "Mitochondrial ribonuclease P protein 2",
                    "type": "synonym"
                },
                {
                    "name": "Short chain dehydrogenase/reductase family 5C member 1",
                    "type": "synonym"
                },
                {
                    "name": "Short-chain type dehydrogenase/reductase XH98G2",
                    "type": "synonym"
                },
                {
                    "name": "Type II HADH",
                    "type": "synonym"
                }
            ],
            "gene_names": [
                {
                    "name": "Hsd17b10",
                    "type": "recommended"
                },
                {
                    "name": "Erab",
                    "type": "synonym"
                },
                {
                    "name": "Hadh2",
                    "type": "synonym"
                }
            ],
            "record_id": "O08756-1",
            "evidence": [
                {
                    "id": "0060810",
                    "database": "AGR",
                    "url": "https://www.alliancegenome.org/disease/DOID:0060810"
                }
            ]
        },
        {
            "uniprot_canonical_ac": "Q99714-1",
            "uniprot_ac": "Q99714",
            "uniprot_id": "HCD2_HUMAN",
            "refseq_ac": "NP_001032900",
            "glycoprotein": "yes",
            "species": [
                {
                    "name": "Homo sapiens",
                    "taxid": 9606,
                    "common_name": "Human",
                    "glygen_name": "Human",
                    "reference_species": "Homo sapiens [9606]"
                }
            ],
            "protein_names": [
                {
                    "name": "3-hydroxyacyl-CoA dehydrogenase type-2",
                    "type": "recommended"
                },
                {
                    "name": "1.1.1.159",
                    "type": "synonym"
                },
                {
                    "name": "1.1.1.178",
                    "type": "synonym"
                },
                {
                    "name": "1.1.1.239",
                    "type": "synonym"
                },
                {
                    "name": "1.1.1.35",
                    "type": "synonym"
                },
                {
                    "name": "1.1.1.53",
                    "type": "synonym"
                },
                {
                    "name": "1.1.1.62",
                    "type": "synonym"
                },
                {
                    "name": "17-beta-estradiol 17-dehydrogenase",
                    "type": "synonym"
                },
                {
                    "name": "2-methyl-3-hydroxybutyryl-CoA dehydrogenase",
                    "type": "synonym"
                },
                {
                    "name": "3-alpha-(17-beta)-hydroxysteroid dehydrogenase (NAD(+))",
                    "type": "synonym"
                },
                {
                    "name": "3-hydroxy-2-methylbutyryl-CoA dehydrogenase",
                    "type": "synonym"
                },
                {
                    "name": "3-hydroxyacyl-CoA dehydrogenase type II",
                    "type": "synonym"
                },
                {
                    "name": "3-hydroxyacyl-CoA dehydrogenase type-2 isoform 2",
                    "type": "synonym"
                },
                {
                    "name": "3alpha(or 20beta)-hydroxysteroid dehydrogenase",
                    "type": "synonym"
                },
                {
                    "name": "7-alpha-hydroxysteroid dehydrogenase",
                    "type": "synonym"
                },
                {
                    "name": "AB-binding alcohol dehydrogenase",
                    "type": "synonym"
                },
                {
                    "name": "Endoplasmic reticulum-associated amyloid beta-peptide-binding protein",
                    "type": "synonym"
                },
                {
                    "name": "MHBD",
                    "type": "synonym"
                },
                {
                    "name": "Mitochondrial RNase P protein 2",
                    "type": "synonym"
                },
                {
                    "name": "Mitochondrial ribonuclease P protein 2",
                    "type": "synonym"
                },
                {
                    "name": "Short chain dehydrogenase/reductase family 5C member 1",
                    "type": "synonym"
                },
                {
                    "name": "Short-chain type dehydrogenase/reductase XH98G2",
                    "type": "synonym"
                },
                {
                    "name": "Type II HADH",
                    "type": "synonym"
                },
                {
                    "name": "amyloid-beta peptide binding alcohol dehydrogenase",
                    "type": "synonym"
                },
                {
                    "name": "endoplasmic reticulum-associated amyloid beta-peptide-binding protein",
                    "type": "synonym"
                },
                {
                    "name": "mitochondrial RNase P subunit 2",
                    "type": "synonym"
                },
                {
                    "name": "mitochondrial ribonuclease P protein 2",
                    "type": "synonym"
                },
                {
                    "name": "short chain L-3-hydroxyacyl-CoA dehydrogenase type 2",
                    "type": "synonym"
                },
                {
                    "name": "short chain type dehydrogenase/reductase XH98G2",
                    "type": "synonym"
                }
            ],
            "gene_names": [
                {
                    "name": "HSD17B10",
                    "type": "recommended"
                },
                {
                    "name": "17b-HSD10",
                    "type": "synonym"
                },
                {
                    "name": "ABAD",
                    "type": "synonym"
                },
                {
                    "name": "CAMR",
                    "type": "synonym"
                },
                {
                    "name": "DUPXp11.22",
                    "type": "synonym"
                },
                {
                    "name": "ERAB",
                    "type": "synonym"
                },
                {
                    "name": "HADH2",
                    "type": "synonym"
                },
                {
                    "name": "HCD2",
                    "type": "synonym"
                },
                {
                    "name": "HSD10MD",
                    "type": "synonym"
                },
                {
                    "name": "HSD17B10",
                    "type": "synonym"
                },
                {
                    "name": "MHBD",
                    "type": "synonym"
                },
                {
                    "name": "MRPP2",
                    "type": "synonym"
                },
                {
                    "name": "MRX17",
                    "type": "synonym"
                },
                {
                    "name": "MRX31",
                    "type": "synonym"
                },
                {
                    "name": "MRXS10",
                    "type": "synonym"
                },
                {
                    "name": "SCHAD",
                    "type": "synonym"
                },
                {
                    "name": "SDR5C1",
                    "type": "synonym"
                },
                {
                    "name": "XH98G2",
                    "type": "synonym"
                }
            ],
            "record_id": "Q99714-1",
            "evidence": [
                {
                    "id": "300438",
                    "database": "MIM",
                    "url": "https://www.omim.org/entry/300438"
                },
                {
                    "id": "0060810",
                    "database": "AGR",
                    "url": "https://www.alliancegenome.org/disease/DOID:0060810"
                }
            ]
        },
        {
            "uniprot_canonical_ac": "O70351-1",
            "uniprot_ac": "O70351",
            "uniprot_id": "HCD2_RAT",
            "refseq_ac": "NP_113870",
            "glycoprotein": "yes",
            "species": [
                {
                    "name": "Rattus norvegicus",
                    "taxid": 10116,
                    "common_name": "Rat",
                    "glygen_name": "Rat",
                    "reference_species": "Rattus norvegicus [10116]"
                }
            ],
            "protein_names": [
                {
                    "name": "3-hydroxyacyl-CoA dehydrogenase type-2",
                    "type": "recommended"
                },
                {
                    "name": "1.1.1.159",
                    "type": "synonym"
                },
                {
                    "name": "1.1.1.178",
                    "type": "synonym"
                },
                {
                    "name": "1.1.1.239",
                    "type": "synonym"
                },
                {
                    "name": "1.1.1.35",
                    "type": "synonym"
                },
                {
                    "name": "1.1.1.53",
                    "type": "synonym"
                },
                {
                    "name": "1.1.1.62",
                    "type": "synonym"
                },
                {
                    "name": "17-beta-HSD 10",
                    "type": "synonym"
                },
                {
                    "name": "17-beta-estradiol 17-dehydrogenase",
                    "type": "synonym"
                },
                {
                    "name": "17-beta-hydroxysteroid dehydrogenase 10",
                    "type": "synonym"
                },
                {
                    "name": "17I(2)-hydroxysteroid dehydrogenase type 10",
                    "type": "synonym"
                },
                {
                    "name": "2-methyl-3-hydroxybutyryl-CoA dehydrogenase",
                    "type": "synonym"
                },
                {
                    "name": "3-alpha-(17-beta)-hydroxysteroid dehydrogenase (NAD(+))",
                    "type": "synonym"
                },
                {
                    "name": "3-hydroxy-2-methylbutyryl-CoA dehydrogenase",
                    "type": "synonym"
                },
                {
                    "name": "3-hydroxyacyl-CoA dehydrogenase type II",
                    "type": "synonym"
                },
                {
                    "name": "3-hydroxyacyl-CoA dehydrogenase type-2",
                    "type": "synonym"
                },
                {
                    "name": "3alpha(or 20beta)-hydroxysteroid dehydrogenase",
                    "type": "synonym"
                },
                {
                    "name": "7-alpha-hydroxysteroid dehydrogenase",
                    "type": "synonym"
                },
                {
                    "name": "Endoplasmic reticulum-associated amyloid beta-peptide-binding protein",
                    "type": "synonym"
                },
                {
                    "name": "MHBD",
                    "type": "synonym"
                },
                {
                    "name": "Mitochondrial RNase P protein 2",
                    "type": "synonym"
                },
                {
                    "name": "Mitochondrial ribonuclease P protein 2",
                    "type": "synonym"
                },
                {
                    "name": "Short chain dehydrogenase/reductase family 5C member 1",
                    "type": "synonym"
                },
                {
                    "name": "Short-chain type dehydrogenase/reductase XH98G2",
                    "type": "synonym"
                },
                {
                    "name": "Type II HADH",
                    "type": "synonym"
                },
                {
                    "name": "amyloid beta-peptide binding protein",
                    "type": "synonym"
                },
                {
                    "name": "amyloid-beta peptide binding alcohol dehydrogenase",
                    "type": "synonym"
                },
                {
                    "name": "endoplasmic reticulum-associated amyloid beta-peptide-binding protein",
                    "type": "synonym"
                },
                {
                    "name": "hydroxyacyl-Coenzyme A dehydrogenase, type II",
                    "type": "synonym"
                },
                {
                    "name": "mitochondrial RNase P protein 2",
                    "type": "synonym"
                },
                {
                    "name": "mitochondrial ribonuclease P protein 2",
                    "type": "synonym"
                },
                {
                    "name": "short chain L-3-hydroxyacyl-CoA dehydrogenase",
                    "type": "synonym"
                },
                {
                    "name": "short chain dehydrogenase/reductase family 5C member 1",
                    "type": "synonym"
                },
                {
                    "name": "short-chain type dehydrogenase/reductase XH98G2",
                    "type": "synonym"
                },
                {
                    "name": "type II HADH",
                    "type": "synonym"
                }
            ],
            "gene_names": [
                {
                    "name": "Hsd17b10",
                    "type": "recommended"
                },
                {
                    "name": "ABAD",
                    "type": "synonym"
                },
                {
                    "name": "ERAB",
                    "type": "synonym"
                },
                {
                    "name": "Erab",
                    "type": "synonym"
                },
                {
                    "name": "HSD10",
                    "type": "synonym"
                },
                {
                    "name": "Hadh2",
                    "type": "synonym"
                },
                {
                    "name": "Hsd17b10",
                    "type": "synonym"
                },
                {
                    "name": "MHBD",
                    "type": "synonym"
                }
            ],
            "record_id": "O70351-1",
            "evidence": [
                {
                    "id": "0060810",
                    "database": "AGR",
                    "url": "https://www.alliancegenome.org/disease/DOID:0060810"
                }
            ]
        },
        {
            "uniprot_canonical_ac": "O18404-1",
            "uniprot_ac": "O18404",
            "uniprot_id": "HCD2_DROME",
            "refseq_ac": "NP_523396",
            "glycoprotein": "no",
            "species": [
                {
                    "name": "Drosophila melanogaster",
                    "taxid": 7227,
                    "common_name": "Fruit fly",
                    "glygen_name": "Fruit fly",
                    "reference_species": "Drosophila melanogaster [7227]"
                }
            ],
            "protein_names": [
                {
                    "name": "3-hydroxyacyl-CoA dehydrogenase type-2",
                    "type": "recommended"
                },
                {
                    "name": "1.1.1.-",
                    "type": "synonym"
                },
                {
                    "name": "1.1.1.35",
                    "type": "synonym"
                },
                {
                    "name": "1.1.1.51",
                    "type": "synonym"
                },
                {
                    "name": "1.1.1.53",
                    "type": "synonym"
                },
                {
                    "name": "1.1.1.62",
                    "type": "synonym"
                },
                {
                    "name": "17-beta-HSD 10",
                    "type": "synonym"
                },
                {
                    "name": "17-beta-hydroxysteroid dehydrogenase 10 ortholog",
                    "type": "synonym"
                },
                {
                    "name": "17-beta-hydroxysteroid dehydrogenase 10",
                    "type": "synonym"
                },
                {
                    "name": "3-hydroxyacyl-CoA dehydrogenase type II",
                    "type": "synonym"
                },
                {
                    "name": "3-hydroxyacyl-CoA dehydrogenase",
                    "type": "synonym"
                },
                {
                    "name": "CG7113-PA",
                    "type": "synonym"
                },
                {
                    "name": "Hydroxysteroid dehydrogenase",
                    "type": "synonym"
                },
                {
                    "name": "Mitochondrial RNase P protein 2",
                    "type": "synonym"
                },
                {
                    "name": "Mitochondrial ribonuclease P protein 2",
                    "type": "synonym"
                },
                {
                    "name": "Scully protein",
                    "type": "synonym"
                },
                {
                    "name": "Type II HADH",
                    "type": "synonym"
                },
                {
                    "name": "haplo-lethal region II",
                    "type": "synonym"
                },
                {
                    "name": "lethal(1)17Ad",
                    "type": "synonym"
                },
                {
                    "name": "scu-PA",
                    "type": "synonym"
                },
                {
                    "name": "scully, isoform A",
                    "type": "synonym"
                },
                {
                    "name": "scully",
                    "type": "synonym"
                }
            ],
            "gene_names": [
                {
                    "name": "scu",
                    "type": "recommended"
                },
                {
                    "name": "17beta-HSD10",
                    "type": "synonym"
                },
                {
                    "name": "CG7113",
                    "type": "synonym"
                },
                {
                    "name": "Dmel\\CG7113",
                    "type": "synonym"
                },
                {
                    "name": "HL-X",
                    "type": "synonym"
                },
                {
                    "name": "HLII",
                    "type": "synonym"
                },
                {
                    "name": "HSD17B10",
                    "type": "synonym"
                },
                {
                    "name": "MRPP2",
                    "type": "synonym"
                },
                {
                    "name": "Scu",
                    "type": "synonym"
                },
                {
                    "name": "l(1)16Fd",
                    "type": "synonym"
                },
                {
                    "name": "l(1)17Ad",
                    "type": "synonym"
                },
                {
                    "name": "scu",
                    "type": "synonym"
                }
            ],
            "record_id": "O18404-1",
            "evidence": [
                {
                    "id": "0060810",
                    "database": "AGR",
                    "url": "https://www.alliancegenome.org/disease/DOID:0060810"
                }
            ]
        }
    ],
    "glycans": [],
    "biomarkers": [],
    "association_flag": "1000",
    "record_id": "doid.0060810"
}
