{
    "disease_id": "DOID:0060843", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008087", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008087", 
            "name": "polyneuropathy, familial recurrent"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008087", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008087", 
            "name": "current pressure-sensitive neuropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008087", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008087", 
            "name": "familial recurrent polyneuropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008087", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008087", 
            "name": "heterozygous microdeletion 17p11.2p12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008087", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008087", 
            "name": "potato-grubbing palsy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008087", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008087", 
            "name": "Tomaculous neuropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008087", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008087", 
            "name": "tulip-bulb digger's palsy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008087", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008087", 
            "name": "neuropathy, hereditary, with liability to pressure palsies; HNPP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008087", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008087", 
            "name": "neuropathy, hereditary, with liability to pressure palsies"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008087", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008087", 
            "name": "hereditary neuropathy with liability to pressure palsy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008087", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008087", 
            "name": "HNPP"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060843", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060843", 
            "name": "HNPP"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060843", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060843", 
            "name": "current pressure-sensitive neuropathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060843", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060843", 
            "name": "familial recurrent polyneuropathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060843", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060843", 
            "name": "heterozygous microdeletion 17p11.2p12"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060843", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060843", 
            "name": "potato-grubbing palsy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060843", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060843", 
            "name": "tomaculous neuropathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060843", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060843", 
            "name": "tulip-bulb digger's palsy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060843", 
        "description": "A neuropathy characterized by autosomal dominant inheritance of peroneal muscle weakness, peripheral neuropathy, hyporeflexia, tomacula, segmental demyelination/remyelination, decreased motor nerve conduction that has_material_basis_in deletion or point mutation of the PMP22 gene on chromosome 17p12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060843", 
        "name": "hereditary neuropathy with liability to pressure palsies"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060843#disease-associations", 
            "id": "0060843", 
            "database": "Alliance of Genome Resources"
        }
    ]
}