{
    "disease_id": "DOID:0060464", 
    "synonyms": [
        {
            "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": "microcephaly-digital anomalies-normal intelligence 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": "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": "digital anomalies with short palpebral fissures and atresia of esophagus or duodenum"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060464", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060464", 
            "name": "microcephaly-oculo-digito-esophageal-duodenal syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013691", 
            "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; see this term) but that lacks the manifestations of gastrointestinal atresia and short palpebral fissures.", 
            "resource": "MONDO", 
            "id": "MONDO:0013691", 
            "name": "Feingold syndrome type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013691", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013691", 
            "name": "Brunner-Winter syndrome type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013691", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013691", 
            "name": "brachydactyly with short stature and microcephaly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013691", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013691", 
            "name": "Feingold syndrome 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013691", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013691", 
            "name": "Feingold syndrome type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013691", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013691", 
            "name": "Feingold syndrome 2; FGLDS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013691", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013691", 
            "name": "microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013691", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013691", 
            "name": "FS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013691", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013691", 
            "name": "brachydactyly-short stature-microcephaly syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013691", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013691", 
            "name": "MMT type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013691", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013691", 
            "name": "FGLDS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013691", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013691", 
            "name": "microcephaly-digital anomalies-normal intelligence syndrome type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008115", 
            "description": "Feingold syndrome type 1 (FS1) is a rare inherited malformation syndrome characterized by microcephaly, short stature and numerous digital anomalies.", 
            "resource": "MONDO", 
            "id": "MONDO:0008115", 
            "name": "Feingold syndrome type 1"
        }, 
        {
            "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": "Feingold syndrome 1; FGLDS1"
        }, 
        {
            "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": "MODED 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": "oculodigitoesophagoduodenal syndrome"
        }, 
        {
            "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": "microcephaly-oculo-digito-esophageal-duodenal syndrome"
        }, 
        {
            "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": "Feingold 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": "oculo-digito-esophageal-duodenal syndrome type 1"
        }, 
        {
            "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": "Mmt syndrome"
        }, 
        {
            "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": "MMT 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": "Feingold syndrome 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": "FS1"
        }, 
        {
            "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": "microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 1"
        }, 
        {
            "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": "microcephaly and digital abnormalities with Normal intelligence"
        }, 
        {
            "url": "https://www.omim.org/entry/614326", 
            "description": "Feingold syndrome 2", 
            "resource": "MIM", 
            "id": "MIM:614326", 
            "name": "Feingold syndrome 2"
        }, 
        {
            "url": "https://www.omim.org/entry/164280", 
            "description": "Feingold syndrome 1", 
            "resource": "MIM", 
            "id": "MIM:164280", 
            "name": "Feingold syndrome 1"
        }
    ], 
    "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"
    }
}