{
    "disease_id": "DOID:0060843",
    "recommended_name": {
        "id": "DOID:0060843",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060843",
        "name": "hereditary neuropathy with liability to pressure palsies",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0060843",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060843",
            "name": "HNPP",
            "description": ""
        },
        {
            "id": "DOID:0060843",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060843",
            "name": "current pressure-sensitive neuropathy",
            "description": ""
        },
        {
            "id": "DOID:0060843",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060843",
            "name": "familial recurrent polyneuropathy",
            "description": ""
        },
        {
            "id": "DOID:0060843",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060843",
            "name": "heterozygous microdeletion 17p11.2p12",
            "description": ""
        },
        {
            "id": "DOID:0060843",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060843",
            "name": "potato-grubbing palsy",
            "description": ""
        },
        {
            "id": "DOID:0060843",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060843",
            "name": "tomaculous neuropathy",
            "description": ""
        },
        {
            "id": "DOID:0060843",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060843",
            "name": "tulip-bulb digger's palsy",
            "description": ""
        },
        {
            "id": "MONDO:0008087",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008087",
            "name": "hereditary neuropathy with liability to pressure palsies",
            "description": "Hereditary neuropathy with liability to pressure palsies (HNPP) is an inherited peripheral nerve disorder characterized by recurrent mononeuropathy usually triggered by minor physical activities."
        },
        {
            "id": "MONDO:0008087",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008087",
            "name": "HNPP",
            "description": ""
        },
        {
            "id": "MONDO:0008087",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008087",
            "name": "Tomaculous neuropathy",
            "description": ""
        },
        {
            "id": "MONDO:0008087",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008087",
            "name": "current pressure-sensitive neuropathy",
            "description": ""
        },
        {
            "id": "MONDO:0008087",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008087",
            "name": "hereditary liability to pressure palsies",
            "description": ""
        },
        {
            "id": "MONDO:0008087",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008087",
            "name": "hereditary neuropathy with liability to pressure palsies",
            "description": ""
        },
        {
            "id": "MONDO:0008087",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008087",
            "name": "heterozygous microdeletion 17p11.2p12",
            "description": ""
        },
        {
            "id": "MONDO:0008087",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008087",
            "name": "neuropathy, recurrent, with pressure palsies",
            "description": ""
        },
        {
            "id": "MONDO:0008087",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008087",
            "name": "potato-grubbing palsy",
            "description": ""
        },
        {
            "id": "MONDO:0008087",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008087",
            "name": "tomaculous neuropathy",
            "description": ""
        },
        {
            "id": "MONDO:0008087",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008087",
            "name": "tulip-bulb digger's palsy",
            "description": ""
        },
        {
            "id": "MONDO:0008087",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008087",
            "name": "hereditary neuropathy with liability to pressure palsy",
            "description": ""
        },
        {
            "id": "MONDO:0008087",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008087",
            "name": "neuropathy, hereditary, with liability to pressure palsies",
            "description": ""
        },
        {
            "id": "MIM:162500",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/162500",
            "name": "Hereditary neuropathy with liability to pressure palsies",
            "description": "Hereditary neuropathy with liability to pressure palsies"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060843"
    ],
    "unlinked_id_list": []
}