{
    "disease_id": "DOID:0050460", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008684", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008684", 
            "name": "WHS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008684", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008684", 
            "name": "chromosome 4p16.3 deletion syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008684", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008684", 
            "name": "4p syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008684", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008684", 
            "name": "4p deletion syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008684", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008684", 
            "name": "Wittwer syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008684", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008684", 
            "name": "distal monosomy 4p"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008684", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008684", 
            "name": "Wolf syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008684", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008684", 
            "name": "Pitt syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008684", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008684", 
            "name": "Pitt-Rogers-Danks syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008684", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008684", 
            "name": "4p- syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008684", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008684", 
            "name": "chromosome 4p syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008684", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008684", 
            "name": "WOLF-Hirschhorn syndrome; WHS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008684", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008684", 
            "name": "distal deletion 4p"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008684", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008684", 
            "name": "telomeric deletion 4p"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008684", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008684", 
            "name": "microcephaly, IUGR, hypertelorism, ptosis, iris coloboma, hooked nose, external ear dysplasia, psychomotor retardation"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050460", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050460", 
            "name": "4p deletion syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050460", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050460", 
            "name": "PITT SYNDROME"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050460", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050460", 
            "name": "Pitt-Rogers-Danks Syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050460", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050460", 
            "name": "chromosome 4p16.3 deletion syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050460", 
        "description": "A chromosomal deletion syndrome that is characterized by distinct craniofacial features, hypotonia and intellectual disability and has_material_basis_in a microdeletion of the short arm of chromosome 4.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050460", 
        "name": "Wolf-Hirschhorn syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050460#disease-associations", 
            "id": "0050460", 
            "database": "Alliance of Genome Resources"
        }
    ]
}