{
    "disease_id": "DOID:12580",
    "recommended_name": {
        "id": "DOID:12580",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:12580",
        "name": "Cri-Du-Chat syndrome",
        "description": "A syndrome that has_material_basis_in deletion of the end of the chromosome 5 p arm and that is characterized by intellectual disability, delayed development, small head size, low birth weight, weak muscle tone widely set eyes, low-set ears, a small jaw, a rounded face and a high-pitched cry that sounds like that of a cat."
    },
    "synonyms": [
        {
            "id": "DOID:12580",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:12580",
            "name": "5p deletion syndrome",
            "description": ""
        },
        {
            "id": "DOID:12580",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:12580",
            "name": "5p partial monosomy syndrome",
            "description": ""
        },
        {
            "id": "DOID:12580",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:12580",
            "name": "Cri-du-chat syndrome",
            "description": ""
        },
        {
            "id": "DOID:12580",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:12580",
            "name": "chromosome 5 short arm deletion syndrome",
            "description": ""
        },
        {
            "id": "DOID:12580",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:12580",
            "name": "chromosome 5p deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007404",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007404",
            "name": "Cri-du-chat syndrome",
            "description": "Monosomy 5p, also known as Cri du chat syndrome, is a rare autosomal deletion syndrome characterized by a mewing cry (cri du chat) in infancy, multiple congenital anomalies, intellectual disability, microcephaly, and facial dysmorphism."
        },
        {
            "id": "MONDO:0007404",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007404",
            "name": "deletion 5p",
            "description": ""
        },
        {
            "id": "MONDO:0007404",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007404",
            "name": "monosomy 5p",
            "description": ""
        },
        {
            "id": "MONDO:0007404",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007404",
            "name": "chromosome 5p- syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007404",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007404",
            "name": "5p minus syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007404",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007404",
            "name": "5p partial monosomy syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007404",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007404",
            "name": "chromosome 5p deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007404",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007404",
            "name": "5p deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007404",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007404",
            "name": "chromosome 5P deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007404",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007404",
            "name": "Cat-Cry syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007404",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007404",
            "name": "Cri-du-chat syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007404",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007404",
            "name": "monosomy type 5p",
            "description": ""
        },
        {
            "id": "MONDO:0007404",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007404",
            "name": "5p- syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007404",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007404",
            "name": "chromosome 5 short arm deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007404",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007404",
            "name": "Cri du chat syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007404",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007404",
            "name": "Cat Cry syndrome",
            "description": ""
        }
    ]
}