{
    "disease_id": "DOID:0060731", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008852", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008852", 
            "name": "ondine's curse (formerly)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008852", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008852", 
            "name": "congenital ondine curse"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008852", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008852", 
            "name": "Haddad syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008852", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008852", 
            "name": "ondine curse, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008852", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008852", 
            "name": "central hypoventilation syndrome, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008852", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008852", 
            "name": "ondine curse (formerly)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008852", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008852", 
            "name": "autonomic control, congenital failure of"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008852", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008852", 
            "name": "ondine syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008852", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008852", 
            "name": "ondine curse"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008852", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008852", 
            "name": "Cchs with Hirschsprung disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008852", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008852", 
            "name": "CCHS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008852", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008852", 
            "name": "primary alveolar hypoventilation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008852", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008852", 
            "name": "ondine-Hirschsprung disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008852", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008852", 
            "name": "congenital failure of autonomic control"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008852", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008852", 
            "name": "central congenital hypoventilation syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008852", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008852", 
            "name": "congenital central alveolar hypoventilation syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008852", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008852", 
            "name": "idiopathic congenital central alveolar hypoventilation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008852", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008852", 
            "name": "central hypoventilation syndrome, congenital; CCHS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008852", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008852", 
            "name": "congenital central hypoventilation"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060731", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060731", 
            "name": "congenital central alveolar hypoventilation syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060731", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060731", 
            "name": "CCHS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060731", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060731", 
            "name": "Ondine curse"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060731", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060731", 
            "name": "Ondine syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060731", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060731", 
            "name": "central congenital hypoventilation syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060731", 
        "description": "An autonomic nervous system disease characterized by reduced responsiveness of the  respiratory center to carbon dioxide, diminished pupillary light responses, and other symptoms related to defects in the autonomic nervous system and that has_material_basis_in most commonly heterozygous mutation in the PHOX2B gene on chromosome 4p13 and less frequently mutations in the RET, GDNF, EDN3, BDNF, or ASCL1 genes.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060731", 
        "name": "congenital central hypoventilation syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060731#disease-associations", 
            "id": "0060731", 
            "database": "Alliance of Genome Resources"
        }
    ]
}