{
    "disease_id": "DOID:0060883", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011176", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011176", 
            "name": "hypomagnesemia caused by selective magnesium malabsorption"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011176", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011176", 
            "name": "TRPM6 familial primary hypomagnesemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011176", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011176", 
            "name": "HSH"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011176", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011176", 
            "name": "PHSH"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011176", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011176", 
            "name": "hypomagnesemia intestinal type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011176", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011176", 
            "name": "intestinal hypomagnesemia with secondary hypocalcemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011176", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011176", 
            "name": "hypomagnesemia 1, intestinal; HOMG1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011176", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011176", 
            "name": "primary hypomagnesemia with secondary hypocalcemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011176", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011176", 
            "name": "intestinal hypomagnesemia type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011176", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011176", 
            "name": "hypomagnesemia with secondary hypocalcemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011176", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011176", 
            "name": "hypomagnesemia, intestinal, with secondary hypocalcemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011176", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011176", 
            "name": "HOMG1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011176", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011176", 
            "name": "familial primary hypomagnesemia caused by mutation in TRPM6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011176", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011176", 
            "name": "Homg"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011176", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011176", 
            "name": "hypomagnesemic tetany"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011176", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011176", 
            "name": "primary hypomagnesemia caused by mutation in TRPM6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011176", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011176", 
            "name": "hypomagnesemia 1, intestinal"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011176", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011176", 
            "name": "TRPM6 primary hypomagnesemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060883", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060883", 
            "name": "HOMG1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060883", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060883", 
            "name": "hypomagnesemia caused by selective magnesium malabsorption"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060883", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060883", 
            "name": "hypomagnesemia intestinal type 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060883", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060883", 
            "name": "hypomagnesemic tetany"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060883", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060883", 
            "name": "primary hypomagnesemia with secondary hypocalcemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060883", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060883", 
            "name": "intestinal hypomagnesemia with secondary hypocalcemia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060883", 
        "description": "A hypomagnesemia characterized by very low serum magnesium levels due to defects in intestinal absorbtion and kidney excretion and secondary hypocalcemia that has material_basis_in homozygous or compound heterozygous mutations in the TRPM6 gene on chromosome 9q21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060883", 
        "name": "intestinal hypomagnesemia 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060883#disease-associations", 
            "id": "0060883", 
            "database": "Alliance of Genome Resources"
        }
    ]
}