{
    "disease_id": "DOID:0111704",
    "recommended_name": {
        "id": "DOID:0111704",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111704",
        "name": "chromosome 2q37 deletion syndrome",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0111704",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111704",
            "name": "2q37 microdeletion syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111704",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111704",
            "name": "Albright hereditary osteodystrophy-like syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111704",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111704",
            "name": "BDMR",
            "description": ""
        },
        {
            "id": "DOID:0111704",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111704",
            "name": "Albright hereditary osteodystrophy type 3",
            "description": ""
        },
        {
            "id": "DOID:0111704",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111704",
            "name": "Albright's hereditary osteodystrophy-like syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111704",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111704",
            "name": "Brachydactyly-intellectual disability syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111704",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111704",
            "name": "Del(2)(q37)",
            "description": ""
        },
        {
            "id": "DOID:0111704",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111704",
            "name": "deletion 2q37",
            "description": ""
        },
        {
            "id": "DOID:0111704",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111704",
            "name": "monosomy 2q37qter",
            "description": ""
        },
        {
            "id": "MONDO:0010886",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010886",
            "name": "2q37 microdeletion syndrome",
            "description": "Deletion 2q37 or monosomy 2q37 is a chromosomal anomaly involving deletion of chromosome band 2q37 and manifests as three major clinical findings: developmental delay, skeletal malformations and facial dysmorphism."
        },
        {
            "id": "MONDO:0010886",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010886",
            "name": "Albright hereditary osteodystrophy type 3",
            "description": ""
        },
        {
            "id": "MONDO:0010886",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010886",
            "name": "brachydactyly mental retardation syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010886",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010886",
            "name": "brachydactyly-intellectual disability syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010886",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010886",
            "name": "Albright hereditary osteodystrophy-like syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010886",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010886",
            "name": "2q37 deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010886",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010886",
            "name": "BDMR",
            "description": ""
        },
        {
            "id": "MONDO:0010886",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010886",
            "name": "chromosome 2q37 deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010886",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010886",
            "name": "brachydactyly-mental retardation syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010886",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010886",
            "name": "Del(2)(q37)",
            "description": ""
        },
        {
            "id": "MONDO:0010886",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010886",
            "name": "deletion 2q37-qter",
            "description": ""
        },
        {
            "id": "MONDO:0010886",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010886",
            "name": "monosomy 2q37-qter",
            "description": ""
        },
        {
            "id": "MONDO:0010886",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010886",
            "name": "deletion 2q37",
            "description": ""
        }
    ]
}