{
    "disease_id": "DOID:0060410", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011929", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011929", 
            "name": "monosomy 1P36 syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011929", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011929", 
            "name": "monosomy 1p36"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011929", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011929", 
            "name": "1p Telomere Deletion syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011929", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011929", 
            "name": "deletion 1p36"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011929", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011929", 
            "name": "deletion 1pter"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011929", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011929", 
            "name": "1p36 deletion syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011929", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011929", 
            "name": "monosomy 1pter"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011929", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011929", 
            "name": "subtelomeric 1p36 deletion"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011929", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011929", 
            "name": "Del(1)(p36)"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060410", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060410", 
            "name": "1p36 deletion syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060410", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060410", 
            "name": "deletion 1p36"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060410", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060410", 
            "name": "monosomy 1p36"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060410", 
        "description": "A chromosomal deletion syndrome that has_material_basis_in by deletion of the chromosome 1p36 region and is characterized by severe intellectual disability, a small head, deep-set eyes with straight eyebrows, midface hypoplasia, a broad, flat nose, a pointed chin and low-set ears.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060410", 
        "name": "chromosome 1p36 deletion syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060410#disease-associations", 
            "id": "0060410", 
            "database": "Alliance of Genome Resources"
        }
    ]
}