{
    "disease_id": "DOID:0080067",
    "recommended_name": {
        "id": "DOID:0080067",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080067",
        "name": "Charcot-Marie-Tooth disease type 5",
        "description": "A Charcot-Marie-Tooth disease that is characterized by pyramidal features including extensor plantar responses, mild increase in tone, and preserved or increased reflexes but no spastic gait."
    },
    "synonyms": [
        {
            "id": "DOID:0080067",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0080067",
            "name": "hereditary motor and sensory neuropathy with pyramidal features",
            "description": ""
        },
        {
            "id": "MONDO:0010877",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010877",
            "name": "Charcot-Marie-Tooth disease type 5",
            "description": "Hereditary motor and sensory neuropathy type 5 is a rare axonal hereditary motor and sensory neuropathy characterized by slowly progressive distal muscle weakness and atrophy with or without sensory loss resulting in difficulty in walking, foot drop and pes cavus, that may be associated with pyramidal signs (extensor plantar responses, mild increase in tone, brisk tendon reflexes), muscle cramps, pain and spasticity."
        },
        {
            "id": "MONDO:0010877",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010877",
            "name": "hereditary motor and sensory neuropathy 5",
            "description": ""
        },
        {
            "id": "MONDO:0010877",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010877",
            "name": "CMT with pyramidal features",
            "description": ""
        },
        {
            "id": "MONDO:0010877",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010877",
            "name": "Hmsn5",
            "description": ""
        },
        {
            "id": "MONDO:0010877",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010877",
            "name": "hereditary motor and sensory neuropathy type 5",
            "description": ""
        },
        {
            "id": "MONDO:0010877",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010877",
            "name": "Charcot-Marie-Tooth neuropathy with pyramidal features, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0010877",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010877",
            "name": "HMSN 5",
            "description": ""
        },
        {
            "id": "MONDO:0010877",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010877",
            "name": "hereditary motor and sensory neuropathy with pyramidal features",
            "description": ""
        },
        {
            "id": "MONDO:0010877",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010877",
            "name": "peroneal muscular atrophy with pyramidal features, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0010877",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010877",
            "name": "hereditary motor and sensory neuropathy V",
            "description": ""
        },
        {
            "id": "MONDO:0010877",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010877",
            "name": "Charcot-Marie-Tooth disease-pyramidal features syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010877",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010877",
            "name": "Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant",
            "description": ""
        }
    ]
}