{
    "disease_id": "DOID:0060810", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010327", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010327", 
            "name": "HSD10 disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010327", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010327", 
            "name": "2-Methyl-3-hydroxybutyryl-Coa dehydrogenase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010327", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010327", 
            "name": "3H2MBD deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010327", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010327", 
            "name": "17 beta-hydroxysteroid dehydrogenase type 10 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010327", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010327", 
            "name": "2-methyl-3-hydroxybutyric aciduria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010327", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010327", 
            "name": "3-hydroxy-2-methylbutyryl-CoA dehydrogenase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010327", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010327", 
            "name": "3-hydroxyacyl-Coa dehydrogenase 2 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010327", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010327", 
            "name": "HSD10 mitochondrial disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010327", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010327", 
            "name": "HSD10MD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010327", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010327", 
            "name": "17-BETA-hydroxysteroid dehydrogenase X deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010327", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010327", 
            "name": "2M3HBA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010327", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010327", 
            "name": "17-Beta-hydroxysteroid dehydrogenase 10 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010327", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010327", 
            "name": "MHBD deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010327", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010327", 
            "name": "HSD10 mitochondrial disease; HSD10MD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010327", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010327", 
            "name": "HSD10 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010327", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010327", 
            "name": "hydroxyacyl-CoA dehydrogenase II deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010327", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010327", 
            "name": "Hsd17B10 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060810", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060810", 
            "name": "HSD10 deficiency, atypical type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060810", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060810", 
            "name": "HSD10 disease, atypical type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060810", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060810", 
            "name": "MRXS10"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060810", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060810", 
            "name": "X-linked intellectual disability-choreoathetosis-abnormal behavior syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060810", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060810", 
            "name": "mental retardation, X-linked syndromic 10"
        }, 
        {
            "url": "https://www.omim.org/entry/300438", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:300438", 
            "name": "HDS10 mitochondrial disease"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060810", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060810", 
        "name": "syndromic X-linked intellectual disability type 10"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/300438", 
            "id": "300438", 
            "database": "MIM"
        }
    ]
}