{
    "disease_id": "DOID:0060885", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007937", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007937", 
            "name": "isolated autosomal dominant hypomagnesemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007937", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007937", 
            "name": "magnesium wasting, renal"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007937", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007937", 
            "name": "isolated renal magnesium wasting"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007937", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007937", 
            "name": "hypomagnesemia 2, renal"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007937", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007937", 
            "name": "magnesium loss, isolated renal"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007937", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007937", 
            "name": "HOMG2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007937", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007937", 
            "name": "familial primary hypomagnesemia caused by mutation in FXYD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007937", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007937", 
            "name": "primary hypomagnesemia caused by mutation in FXYD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007937", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007937", 
            "name": "autosomal dominant primary hypomagnesemia with hypocalciuria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007937", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007937", 
            "name": "FXYD2 primary hypomagnesemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007937", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007937", 
            "name": "FXYD2 familial primary hypomagnesemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007937", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007937", 
            "name": "renal hypomagnesemia type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007937", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007937", 
            "name": "hypomagnesemia 2, renal; HOMG2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060885", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060885", 
            "name": "HOMG2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060885", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060885", 
            "name": "autosomal dominant primary hypomagnesemia with hypocalciuria"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060885", 
        "description": "A hypomagnesemia characterized by autosomal dominant inheritance of hypomagnesemia due to renal magnesium loss that has material_basis_in heterozygous mutation in the FXYD2 gene on chromosome 11q23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060885", 
        "name": "renal hypomagnesemia 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060885#disease-associations", 
            "id": "0060885", 
            "database": "Alliance of Genome Resources"
        }
    ]
}