{
    "disease_id": "DOID:0060347",
    "recommended_name": {
        "id": "DOID:0060347",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060347",
        "name": "acrorenal syndrome",
        "description": "A syndrome characterized by limb defects, usually bilateral, like cleft hands or feet and longitudinal defects involving radius or ulna, tibia or fibula and renal anomalies which include agenesis, hypoplasia and rarely polycystic kidneys. Additional malformations may involve the oro-mandibular region, the trachea and lungs, skin derivatives including sweat glands, mammary glands, the uterus, vas deferens, the nasal placodes and the eyes."
    },
    "synonyms": [
        {
            "id": "MONDO:0008719",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008719",
            "name": "acrorenal syndrome, autosomal recessive",
            "description": "Autosomal recessive form of acrorenal syndrome."
        },
        {
            "id": "MONDO:0008719",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008719",
            "name": "autosomal recessive acrorenal syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008719",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008719",
            "name": "Curran syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008719",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008719",
            "name": "acrorenal syndrome recessive",
            "description": ""
        },
        {
            "id": "MONDO:0008719",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008719",
            "name": "acrorenal syndrome, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0008719",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008719",
            "name": "acrorenal syndrome autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0007059",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007059",
            "name": "acrorenal syndrome",
            "description": "Acrorenal syndrome comprises a wide spectrum of congenital malformative disorders characterized by the co-occurrence of distal limb anomalies (usually bilateral cleft feet and/or hands) and renal defects (e.g. unilateral or bilateral agenesis), that can be associated with a variety of other anomalies such as those of genitourinary tract (genital anomalies, ureteral hypoplasias, vesicoureteral reflux), abdominal well defects, intestinal atresias, and lung malformations. Familial cases have been reported in which an autosomal recessive inheritance was suspected."
        },
        {
            "id": "MONDO:0007059",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007059",
            "name": "acrorenal syndrome",
            "description": ""
        }
    ]
}