{
    "disease_id": "DOID:0060254", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009999", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009999", 
            "name": "autosomal recessive Robinow syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009999", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009999", 
            "name": "costovertebral segmentation defect with mesomelia, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009999", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009999", 
            "name": "costovertebral segmentation defect with mesomelia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009999", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009999", 
            "name": "Robinow syndrome, autosomal recessive; RRS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009999", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009999", 
            "name": "Covesdem syndrome, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009999", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009999", 
            "name": "Robinow syndrome, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009999", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009999", 
            "name": "Covesdem syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009999", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009999", 
            "name": "Robinow syndrome, autosomal recessive, with aplasia/hypoplasia of phalanges and metacarpals/metatarsals"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009999", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009999", 
            "name": "RRS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009999", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009999", 
            "name": "costovertebral segmentation defect-mesomelia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009999", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009999", 
            "name": "Robinow syndrome, autosomal recessive, with Brachy-syn-polydactyly"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060254", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060254", 
            "name": "Robinow dwarfism"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060254", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060254", 
            "name": "fetal face syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060254", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060254", 
            "name": "acral dysostosis with facial and genital abnormalities"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060254", 
        "description": "A syndrome characterized by mild to moderate short stature due to growth delays after birth, distinctive craniofacial abnormalities, skeletal malformations and genital abnormalities.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060254", 
        "name": "Robinow syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060254#disease-associations", 
            "id": "0060254", 
            "database": "Alliance of Genome Resources"
        }
    ]
}