{
    "disease_id": "DOID:0060822", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010306", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010306", 
            "name": "X-linked intellectual disability, Cabezas type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010306", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010306", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010306", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010306", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010306", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010306", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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            "name": "mental retardation, X-linked, with short stature, hypogonadism, and abnormal Gait"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010306", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010306", 
            "name": "X-linked mental retardation with short stature"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010306", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010306", 
            "name": "Cul4B-related X-linked intellectual disability"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010306", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010306", 
            "name": "mental retardation, X-linked, syndromic, Cabezas type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010306", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010306", 
            "name": "mental retardation, X-linked, syndromic 15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010306", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010306", 
            "name": "MRSS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010306", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010306", 
            "name": "Cabezas syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010306", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010306", 
            "name": "MRXSC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010306", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010306", 
            "name": "MRXS15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010306", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010306", 
            "name": "Cabezas syndrome; syndromic X-linked mental retardation 15"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010306", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010306", 
            "name": "Cabezas type of X-linked syndromic intellectual disability"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060822", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060822", 
            "name": "MRSS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060822", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060822", 
            "name": "MRXS15"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060822", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060822", 
            "name": "MRXSC"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060822", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060822", 
            "name": "X-linked mental retardation with short stature"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060822", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060822", 
            "name": "X-linked mental retardation with short stature, hypogonadism, and abnormal gait"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060822", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060822", 
            "name": "mental retardation, X-linked, syndromic 15"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060822", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060822", 
            "name": "Cabezas syndrome; syndromic X-linked mental retardation 15"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060822", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060822", 
            "name": "mental retardation, X-linked, syndromic 15 (Cabezas type)"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060822", 
        "description": "A syndromic X-linked intellectual disability characterized by intellectual deficit, muscle wasting, short stature, hypogonadism, and  bnormal gait, with variable occurrence of prominent lower lip, kyphosis, joint hyperextensibility, tremor, decreased fine motor coordination and impaired speech that has_material_basis_in  mutation in the CUL4B gene on chromosome Xq23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060822", 
        "name": "syndromic X-linked intellectual disability Cabezas type"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060822#disease-associations", 
            "id": "0060822", 
            "database": "Alliance of Genome Resources"
        }
    ]
}