{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010886", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010886", 
            "name": "2q37 microdeletion syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010886", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010886", 
            "name": "Albright hereditary osteodystrophy type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010886", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010886", 
            "name": "brachydactyly mental retardation syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010886", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010886", 
            "name": "brachydactyly-intellectual disability syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010886", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010886", 
            "name": "Albright hereditary osteodystrophy-like syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010886", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010886", 
            "name": "2q37 deletion syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010886", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010886", 
            "name": "BDMR"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010886", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010886", 
            "name": "brachydactyly-mental retardation syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010886", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010886", 
            "name": "Del(2)(q37)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010886", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010886", 
            "name": "deletion 2q37-qter"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010886", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010886", 
            "name": "monosomy 2q37-qter"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010886", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010886", 
            "name": "deletion 2q37"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111704", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111704", 
            "name": "2q37 microdeletion syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111704", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111704", 
            "name": "Albright hereditary osteodystrophy type 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111704", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111704", 
            "name": "Albright hereditary osteodystrophy-like syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111704", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111704", 
            "name": "Albright's hereditary osteodystrophy-like syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111704", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111704", 
            "name": "BDMR"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111704", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111704", 
            "name": "Brachydactyly-intellectual disability syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111704", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111704", 
            "name": "Del(2)(q37)"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111704", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111704", 
            "name": "deletion 2q37"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111704", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111704", 
            "name": "monosomy 2q37qter"
        }, 
        {
            "url": "https://www.omim.org/entry/600430", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:600430", 
            "name": "Brachydactyly-mental retardation syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111704", 
        "description": "A chromosomal deletion syndrome characterized by variable features, likely resulting from different sized deletions, including; brachydactyly type E, short stature, mild to moderate intellectual disability, behavioral abnormalities, and dysmorphic facial features that has_material_basis_in heterozygosity for a contiguous deletion of several genes on chromosome 2q37.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111704", 
        "name": "chromosome 2q37 deletion syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/600430", 
            "id": "600430", 
            "database": "MIM"
        }
    ]
}