{
    "disease_id": "DOID:0060179", 
    "synonyms": [
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            "description": "", 
            "resource": "MONDO", 
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            "name": "mental retardation, X-linked Renpenning type"
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010653", 
            "name": "X-linked intellectual disability, Renpenning type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010653", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010653", 
            "name": "X-linked intellectual disability due to PQBP1 mutations"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010653", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010653", 
            "name": "MRXS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010653", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010653", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010653", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010653", 
            "name": "Golabi-Ito-Hall syndrome"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010653", 
            "name": "Sutherland-Haan syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010653", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010653", 
            "name": "syndromic X-linked mental retardation 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010653", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010653", 
            "name": "X-linked mental retardation with spastic diplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010653", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010653", 
            "name": "Renpenning syndrome 1; RENS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010653", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010653", 
            "name": "mental retardation, X-linked, with spastic diplegia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010653", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010653", 
            "name": "Renpenning syndrome type 1"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010653", 
            "name": "RENS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010653", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010653", 
            "name": "mental retardation, X-linked, syndromic 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010653", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010653", 
            "name": "mental retardation, X-linked 55"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010653", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010653", 
            "name": "MRXS8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010653", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010653", 
            "name": "Sutherland-Haan X-linked mental retardation syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060179", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060179", 
            "name": "Golabi-Ito-Hall syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060179", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060179", 
            "name": "X-linked intellectual disability, Renpenning type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060179", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060179", 
            "name": "X-linked mental retardation Renpenning type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060179", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060179", 
            "name": "X-linked mental retardation with spastic diplegia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060179", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060179", 
            "name": "syndromic X-linked mental retardation 8"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060179", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060179", 
            "name": "X-linked intellectual disability due to PQBP1 mutations"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060179", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060179", 
            "name": "Sutherland-Haan X-linked mental retardation syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060179", 
        "description": "An intellectual disability that is characterized by small head size (microcephaly), long narrow face, short stature, small testes, and intellectual deficit which follows X-linked inheritance and presents most often in males.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060179", 
        "name": "Renpenning syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060179#disease-associations", 
            "id": "0060179", 
            "database": "Alliance of Genome Resources"
        }
    ]
}