{
    "disease_id": "DOID:0050471",
    "recommended_name": {
        "id": "DOID:0050471",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050471",
        "name": "Carney complex",
        "description": "A syndrome characterized by myxomas, spotty pigmentation of the skin and endocrine overactivity."
    },
    "synonyms": [
        {
            "id": "DOID:0050471",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050471",
            "name": "Carney Complex, Type 1",
            "description": ""
        },
        {
            "id": "DOID:0050471",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050471",
            "name": "Carney Complex, Type 2",
            "description": ""
        },
        {
            "id": "DOID:0050471",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050471",
            "name": "Carney Syndrome",
            "description": ""
        },
        {
            "id": "DOID:0050471",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050471",
            "name": "Carney complex variant",
            "description": ""
        },
        {
            "id": "DOID:0050471",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050471",
            "name": "LAMB Syndrome",
            "description": ""
        },
        {
            "id": "DOID:0050471",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050471",
            "name": "NAME Syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008057",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008057",
            "name": "Carney complex, type 1",
            "description": "Any Carney complex in which the cause of the disease is a mutation in the PRKAR1A gene."
        },
        {
            "id": "MONDO:0008057",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008057",
            "name": "Carney complex caused by mutation in PRKAR1A",
            "description": ""
        },
        {
            "id": "MONDO:0008057",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008057",
            "name": "Carney complex, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008057",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008057",
            "name": "PRKAR1A Carney complex",
            "description": ""
        },
        {
            "id": "MONDO:0008057",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008057",
            "name": "CNC1",
            "description": ""
        },
        {
            "id": "MONDO:0011525",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011525",
            "name": "Carney complex type 2",
            "description": ""
        },
        {
            "id": "MONDO:0011525",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011525",
            "name": "CNC2",
            "description": ""
        },
        {
            "id": "MONDO:0011525",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011525",
            "name": "Carney Myxoma-endocrine Complex, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0011525",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011525",
            "name": "Carney complex, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0011525",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011525",
            "name": "Carney complex, type II",
            "description": ""
        },
        {
            "id": "MONDO:0012137",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012137",
            "name": "Carney complex - trismus - pseudocamptodactyly syndrome",
            "description": "Carney complex-trismus-pseudocamptodactyly syndrome is a rare genetic heart-hand syndrome characterized by typical manifestations of the Carney complex (spotty pigmentation of the skin, familial cardiac and cutaneous myxomas and endocrinopathy) associated with trismus and distal arthrogryposis (presenting as involuntary contraction of distal and proximal interphalangeal joints of hands evident only on dorsiflexion of wrist and similar lower-limb contractures producing foot deformities)."
        },
        {
            "id": "MONDO:0012137",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012137",
            "name": "Carney complex variant",
            "description": ""
        },
        {
            "id": "MIM:160980",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/160980",
            "name": "Carney complex 1",
            "description": "Carney complex 1"
        },
        {
            "id": "MIM:608837",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/608837",
            "name": "Carney complex variant",
            "description": "Carney complex variant"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050471"
    ],
    "unlinked_id_list": []
}