{
    "disease_id": "DOID:0060874", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013006", 
            "name": "IGHD 1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013006", 
            "name": "congenital isolated GH deficiency type IB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013006", 
            "name": "isolated growth hormone deficiency type 1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013006", 
            "name": "isolated growth hormone deficiency, type IB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013006", 
            "name": "IGHD IB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013006", 
            "name": "isolated Growth hormone deficiency, type 1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013006", 
            "name": "congenital IGHD type IB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013006", 
            "name": "dwarfism of Sindh"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013006", 
            "name": "congenital isolated growth hormone deficiency type IB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013006", 
            "name": "isolated growth hormone deficiency, type IB; IGHD1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013006", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013006", 
            "name": "IGHD1B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060874", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060874", 
            "name": "IGHD IB"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060874", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060874", 
            "name": "congenital IGHD type IB"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060874", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060874", 
            "name": "congenital isolated GH deficiency type IB"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060874", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060874", 
            "name": "dwarfism of Sindh"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060874", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060874", 
            "name": "congenital isolated growth hormone deficiency type IB"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060874", 
        "description": "An isolated growth hormone deficiency characterized by autosomal recessive inheritance of low but detectable levels of GH, short stature, significantly retarded bone age, and a positive response and immunologic tolerance to growth hormone therapy that has material_basis_in mutation in the GH1 or GHRHR genes on chromosomes 17q23.3 and 7p14.3, respectively.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060874", 
        "name": "isolated growth hormone deficiency type IB"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060874#disease-associations", 
            "id": "0060874", 
            "database": "Alliance of Genome Resources"
        }
    ]
}