{
    "disease_id": "DOID:0050460",
    "recommended_name": {
        "id": "DOID:0050460",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050460",
        "name": "Wolf-Hirschhorn syndrome",
        "description": "A chromosomal deletion syndrome that is characterized by distinct craniofacial features, hypotonia and intellectual disability and has_material_basis_in a hemizygous deletion of chromosome 4p16.3."
    },
    "synonyms": [
        {
            "id": "DOID:0050460",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050460",
            "name": "4p deletion syndrome",
            "description": ""
        },
        {
            "id": "DOID:0050460",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050460",
            "name": "PITT SYNDROME",
            "description": ""
        },
        {
            "id": "DOID:0050460",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050460",
            "name": "Pitt-Rogers-Danks Syndrome",
            "description": ""
        },
        {
            "id": "DOID:0050460",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050460",
            "name": "chromosome 4p16.3 deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008684",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008684",
            "name": "Wolf-Hirschhorn syndrome",
            "description": "Wolf-Hirschhorn syndrome (WHS) is a developmental disorder characterized by typical craniofacial features, prenatal and postnatal growth impairment, intellectual disability, severe delayed psychomotor development, seizures, and hypotonia."
        },
        {
            "id": "MONDO:0008684",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008684",
            "name": "4p deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008684",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008684",
            "name": "4p- syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008684",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008684",
            "name": "Pitt syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008684",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008684",
            "name": "Pitt-Rogers-Danks syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008684",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008684",
            "name": "Wittwer syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008684",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008684",
            "name": "Wolf-Hirschhorn syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008684",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008684",
            "name": "Wolf-Hirschhorn syndrome, Isolated cases",
            "description": ""
        },
        {
            "id": "MONDO:0008684",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008684",
            "name": "chromosome 4p16.3 deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008684",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008684",
            "name": "distal deletion 4p",
            "description": ""
        },
        {
            "id": "MONDO:0008684",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008684",
            "name": "distal monosomy 4p",
            "description": ""
        },
        {
            "id": "MONDO:0008684",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008684",
            "name": "telomeric deletion 4p",
            "description": ""
        },
        {
            "id": "MONDO:0008684",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008684",
            "name": "4p syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008684",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008684",
            "name": "WHS",
            "description": ""
        },
        {
            "id": "MONDO:0008684",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008684",
            "name": "Wolf syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008684",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008684",
            "name": "chromosome 4p syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008684",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008684",
            "name": "microcephaly, IUGR, hypertelorism, ptosis, iris coloboma, hooked nose, external ear dysplasia, psychomotor retardation",
            "description": ""
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050460"
    ],
    "unlinked_id_list": []
}