{
    "disease_id": "DOID:9521", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009877", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009877", 
            "name": "Laron dwarfism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009877", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009877", 
            "name": "growth hormone insensitivity syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009877", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009877", 
            "name": "primary GH resistance"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009877", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009877", 
            "name": "primary GH insensitivity"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009877", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009877", 
            "name": "pituitary dwarfism II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009877", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009877", 
            "name": "Laron-type dwarfism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009877", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009877", 
            "name": "short stature due to growth hormone resistance"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009877", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009877", 
            "name": "Laron-type isolated somatotropin defect"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009877", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009877", 
            "name": "primary growth hormone insensitivity"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009877", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009877", 
            "name": "Growth hormone receptor deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009877", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009877", 
            "name": "primary growth hormone resistance"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009877", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009877", 
            "name": "pituitary dwarfism 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009877", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009877", 
            "name": "Laron type pituitary dwarfism I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009877", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009877", 
            "name": "GH receptor deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009877", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009877", 
            "name": "complete growth hormone insensitivity"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:9521", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:9521", 
            "name": "Laron-type isolated somatotropin defect"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:9521", 
        "description": "A syndrome characterized by marked short stature with normal or high serum growth hormone and low serum insulin-like growth factor-1 levels that has_material_basis_in homozygous or compound heterozygous mutation in GHR on chromosome 5p13-p12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:9521", 
        "name": "Laron syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/262500", 
            "id": "262500", 
            "database": "MIM"
        }
    ]
}