{
    "disease_id": "DOID:0060855",
    "recommended_name": {
        "id": "DOID:0060855",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060855",
        "name": "autosomal dominant pseudohypoaldosteronism type 1",
        "description": "A pseudohypoaldosteronism characterized by Salt wasting resulting from renal unresponsiveness to mineralocorticoids that has_material_basis_in heterozygous mutation in the NR3C2 gene on chromosome 4q31."
    },
    "synonyms": [
        {
            "id": "DOID:0060855",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060855",
            "name": "PHA1A",
            "description": ""
        },
        {
            "id": "DOID:0060855",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060855",
            "name": "autosomal dominant PHA 1",
            "description": ""
        },
        {
            "id": "MONDO:0008329",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008329",
            "name": "autosomal dominant pseudohypoaldosteronism type 1",
            "description": "Renal pseudohypoaldosteronism type 1 (renal PHA1) is a mild form of primary mineralocorticoid resistance restricted to the kidney."
        },
        {
            "id": "MONDO:0008329",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008329",
            "name": "PHA1A",
            "description": ""
        },
        {
            "id": "MONDO:0008329",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008329",
            "name": "autosomal dominant pseudohypoaldosteronism type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008329",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008329",
            "name": "pseudohypoaldosteronism type i, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008329",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008329",
            "name": "pseudohypoaldosteronism type 1 autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008329",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008329",
            "name": "pseudohypoaldosteronism type 1, dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008329",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008329",
            "name": "pseudohypoaldosteronism, type I, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008329",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008329",
            "name": "renal PHA1",
            "description": ""
        },
        {
            "id": "MONDO:0008329",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008329",
            "name": "renal pseudohypoaldosteronism type 1",
            "description": ""
        },
        {
            "id": "MIM:177735",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/177735",
            "name": "Pseudohypoaldosteronism 1, autosomal dominant",
            "description": "Pseudohypoaldosteronism 1, autosomal dominant"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060855"
    ],
    "unlinked_id_list": []
}