{
    "disease_id": "DOID:0060464", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008115", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008115", 
            "name": "Feingold syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008115", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008115", 
            "name": "digital anomalies with short palpebral fissures and atresia of esophagus or duodenum"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008115", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008115", 
            "name": "microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008115", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008115", 
            "name": "FS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008115", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008115", 
            "name": "oculodigitoesophagoduodenal syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008115", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008115", 
            "name": "microcephaly-oculo-digito-esophageal-duodenal syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008115", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008115", 
            "name": "microcephaly-digital anomalies-normal intelligence syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008115", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008115", 
            "name": "Mmt syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008115", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008115", 
            "name": "Oded syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008115", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008115", 
            "name": "FGLDS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008115", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008115", 
            "name": "oculo-digito-esophageal-duodenal syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008115", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008115", 
            "name": "microcephaly and digital abnormalities with Normal intelligence"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008115", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008115", 
            "name": "ODED syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008115", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008115", 
            "name": "Feingold syndrome 1; FGLDS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008115", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008115", 
            "name": "Feingold syndrome 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008115", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008115", 
            "name": "MODED syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008115", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008115", 
            "name": "Feingold syndrome caused by mutation in MYCN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008115", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008115", 
            "name": "Brunner-Winter syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008115", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008115", 
            "name": "microcephaly-oculo-digito-esophageal-duodenal syndrome syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008115", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008115", 
            "name": "MYCN Feingold syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008115", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008115", 
            "name": "digital anomalies with short palpebral fissures and atresia of esophagus or duodenum type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008115", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008115", 
            "name": "microcephaly, mental retardation, and tracheoesophageal fistula syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008115", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008115", 
            "name": "MMT type 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060464", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060464", 
            "name": "microcephaly-oculo-digito-esophageal-duodenal syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060464", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060464", 
            "name": "microcephaly-digital anomalies-normal intelligence syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060464", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060464", 
            "name": "FGLDS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060464", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060464", 
            "name": "MODED syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060464", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060464", 
            "name": "ODED syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060464", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060464", 
            "name": "oculo-digito-esophageal-duodenal syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060464", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060464", 
            "name": "digital anomalies with short palpebral fissures and atresia of esophagus or duodenum"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060464", 
        "description": "A syndrome characterized by variable combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and learning disability/mental retardation.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060464", 
        "name": "Feingold syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060464#disease-associations", 
            "id": "0060464", 
            "database": "Alliance of Genome Resources"
        }
    ]
}