{
    "disease_id": "DOID:0060886", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010310", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010310", 
            "name": "osteopathia striata - cranial sclerosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010310", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010310", 
            "name": "osteopathia striata-cranial sclerosis syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010310", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010310", 
            "name": "hyperostosis generalisata with striations"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010310", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010310", 
            "name": "osteopathia striata with cranial sclerosis; OSCS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010310", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010310", 
            "name": "OSCS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010310", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010310", 
            "name": "osteopathia striata cranial sclerosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010310", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010310", 
            "name": "Robinow-Unger syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060886", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060886", 
            "name": "Robinow-Unger syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060886", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060886", 
            "name": "hyperostosis generalisata with striations"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060886", 
        "description": "An osteosclerosis characterized by longitudinal striations of the metaphyses of the long bones, sclerosis of the craniofacial bones, macrocephaly, cleft palate and hearing loss in females and fetal or neonatal lethality in males that has material_basis_in mutation in the AMER1 gene on chromosome Xq11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060886", 
        "name": "osteopathia striata with cranial sclerosis"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060886#disease-associations", 
            "id": "0060886", 
            "database": "Alliance of Genome Resources"
        }
    ]
}
