{
    "disease_id": "DOID:0060464",
    "recommended_name": {
        "id": "DOID:0060464",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060464",
        "name": "Feingold syndrome",
        "description": "A syndrome characterized by variable combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and learning disability/mental retardation."
    },
    "synonyms": [
        {
            "id": "DOID:0060464",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060464",
            "name": "microcephaly-oculo-digito-esophageal-duodenal syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060464",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060464",
            "name": "microcephaly-digital anomalies-normal intelligence syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060464",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060464",
            "name": "FGLDS",
            "description": ""
        },
        {
            "id": "DOID:0060464",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060464",
            "name": "MODED syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060464",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060464",
            "name": "ODED syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060464",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060464",
            "name": "oculo-digito-esophageal-duodenal syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060464",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060464",
            "name": "digital anomalies with short palpebral fissures and atresia of esophagus or duodenum",
            "description": ""
        },
        {
            "id": "MONDO:0013691",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013691",
            "name": "Feingold syndrome type 2",
            "description": "Feingold syndrome type 2 (FS2) is a rare inherited malformation syndrome characterized by skeletal abnormalities and mild intellectual disabilities similar to those seen in Feingold syndrome type 1 (FS1) but that lacks the manifestations of gastrointestinal atresia and short palpebral fissures."
        },
        {
            "id": "MONDO:0013691",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013691",
            "name": "Brunner-Winter syndrome type 2",
            "description": ""
        },
        {
            "id": "MONDO:0013691",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013691",
            "name": "FGLDS2",
            "description": ""
        },
        {
            "id": "MONDO:0013691",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013691",
            "name": "FS2",
            "description": ""
        },
        {
            "id": "MONDO:0013691",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013691",
            "name": "Feingold syndrome type 2",
            "description": ""
        },
        {
            "id": "MONDO:0013691",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013691",
            "name": "MMT type 2",
            "description": ""
        },
        {
            "id": "MONDO:0013691",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013691",
            "name": "brachydactyly-short stature-microcephaly syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0013691",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013691",
            "name": "microcephaly-digital anomalies-normal intelligence syndrome type 2",
            "description": ""
        },
        {
            "id": "MONDO:0013691",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013691",
            "name": "microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 2",
            "description": ""
        },
        {
            "id": "MONDO:0013691",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013691",
            "name": "Feingold syndrome 2",
            "description": ""
        },
        {
            "id": "MONDO:0013691",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013691",
            "name": "brachydactyly with short stature and microcephaly",
            "description": ""
        },
        {
            "id": "MONDO:0008115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008115",
            "name": "Feingold syndrome type 1",
            "description": "Feingold syndrome type 1 (FS1) is a rare inherited malformation syndrome characterized by microcephaly, short stature and numerous digital anomalies."
        },
        {
            "id": "MONDO:0008115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008115",
            "name": "Brunner-Winter syndrome type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008115",
            "name": "FGLDS1",
            "description": ""
        },
        {
            "id": "MONDO:0008115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008115",
            "name": "FS1",
            "description": ""
        },
        {
            "id": "MONDO:0008115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008115",
            "name": "Feingold syndrome caused by mutation in MYCN",
            "description": ""
        },
        {
            "id": "MONDO:0008115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008115",
            "name": "Feingold syndrome type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008115",
            "name": "MMT type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008115",
            "name": "MODED syndrome type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008115",
            "name": "MYCN Feingold syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008115",
            "name": "ODED syndrome type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008115",
            "name": "digital anomalies with short palpebral fissures and atresia of esophagus or duodenum type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008115",
            "name": "digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008115",
            "name": "microcephaly-digital anomalies-normal intelligence syndrome type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008115",
            "name": "microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008115",
            "name": "microcephaly-oculo-digito-esophageal-duodenal syndrome syndrome type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008115",
            "name": "oculo-digito-esophageal-duodenal syndrome type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008115",
            "name": "Feingold syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008115",
            "name": "Feingold syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0008115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008115",
            "name": "Mmt syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008115",
            "name": "Oded syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008115",
            "name": "digital anomalies with short palpebral fissures and atresia of esophagus or duodenum",
            "description": ""
        },
        {
            "id": "MONDO:0008115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008115",
            "name": "digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum",
            "description": ""
        },
        {
            "id": "MONDO:0008115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008115",
            "name": "microcephaly and digital abnormalities with normal intelligence",
            "description": ""
        },
        {
            "id": "MONDO:0008115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008115",
            "name": "microcephaly, intellectual disability, and tracheoesophageal fistula syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008115",
            "name": "microcephaly, mental retardation, and tracheoesophageal fistula syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008115",
            "name": "microcephaly-oculo-digito-esophageal-duodenal syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008115",
            "name": "oculodigitoesophagoduodenal syndrome",
            "description": ""
        },
        {
            "id": "MIM:614326",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614326",
            "name": "Feingold syndrome 2",
            "description": "Feingold syndrome 2"
        },
        {
            "id": "MIM:164280",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/164280",
            "name": "Feingold syndrome 1",
            "description": "Feingold syndrome 1"
        }
    ]
}