{
    "disease_id": "DOID:0060854", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009917", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009917", 
            "name": "pseudohypoaldosteronism, type I, autosomal recessive; PHA1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009917", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009917", 
            "name": "pseudohypoaldosteronism type 1 autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009917", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009917", 
            "name": "PHA1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009917", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009917", 
            "name": "pseudohypoaldosteronism, type I, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009917", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009917", 
            "name": "autosomal recessive PHA 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009917", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009917", 
            "name": "pseudohypoaldosteronism type 1, recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009917", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009917", 
            "name": "PHA I, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009917", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009917", 
            "name": "generalized pseudohypoaldosteronism type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009917", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009917", 
            "name": "generalized PHA1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060854", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060854", 
            "name": "PHA1B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060854", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060854", 
            "name": "autosomal recessive PHA 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060854", 
        "description": "A pseudohypoaldosteronism characterized by enal salt wasting and high concentrations of sodium in sweat, stool, and saliva that has_material_basis_in homozygous or compound heterozygous mutation in any one of 3 genes encoding subunits of the epithelial sodium channel (ENaC): SCNN1A, SCNN1B, or SCNN1G.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060854", 
        "name": "autosomal recessive pseudohypoaldosteronism type 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060854#disease-associations", 
            "id": "0060854", 
            "database": "Alliance of Genome Resources"
        }
    ]
}