{
    "disease_id": "DOID:0060801", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010258", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010258", 
            "name": "MRXS25"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010258", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010258", 
            "name": "mental retardation, X-linked, syndromic 25"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010258", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010258", 
            "name": "syndromic X-linked mental retardation 20"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010258", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010258", 
            "name": "MRXS20"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010258", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010258", 
            "name": "mental retardation, X-linked, syndromic 20"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010258", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010258", 
            "name": "mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity; MEHMO"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010258", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010258", 
            "name": "X-linked MEHMO syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010258", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010258", 
            "name": "mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010258", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010258", 
            "name": "MEHMO syndrome; MEHMO"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010258", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010258", 
            "name": "MEHMO"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010258", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010258", 
            "name": "intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010258", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010258", 
            "name": "syndromic X-linked mental retardation 25"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010258", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010258", 
            "name": "X-linked intellectual disability-epileptic seizures-hypogenitalism-microcephaly-obesity syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060801", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060801", 
            "name": "X-linked intellectual disability-epileptic seizures-hypogenitalism-microcephaly-obesity syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060801", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060801", 
            "name": "MRXS20"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060801", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060801", 
            "name": "MRXS25"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060801", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060801", 
            "name": "syndromic X-linked mental retardation 20"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060801", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060801", 
            "name": "syndromic X-linked mental retardation 25"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060801", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060801", 
            "name": "mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060801", 
        "description": "A syndromic X-linked intellectual disability characterized by severe intellectual deficit, epilepsy, microcephaly, hypogenitalism and obesity with variable occurrence of growth delay and diabetes that has_material_basis_in variation in the chromosome region Xp22.13-p21.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060801", 
        "name": "MEHMO syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060801#disease-associations", 
            "id": "0060801", 
            "database": "Alliance of Genome Resources"
        }
    ]
}