{
    "disease_id": "DOID:0111371", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007747", 
            "name": "Hyperchlorhidrosis, isolated"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111371", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111371", 
            "name": "HYCHL"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111371", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111371", 
            "name": "carbonic anhydrase XII deficiency"
        }, 
        {
            "url": "https://www.omim.org/entry/143860", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:143860", 
            "name": "Hyperchlorhidrosis, isolated"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111371", 
        "description": "A skin disease characterized by excessive loss of salt in sweat resulting in low levels of salt in the blood in the absence of other symptoms that has_material_basis_in homozygous or compound heterozygous mutation in CA12 on chromosome 15q22.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111371", 
        "name": "isolated hyperchlorhidrosis"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/143860", 
            "id": "143860", 
            "database": "MIM"
        }
    ]
}