{
    "disease_id": "DOID:0060873", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009876", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009876", 
            "name": "Growth hormone deficiency, isolated autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009876", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009876", 
            "name": "isolated Growth hormone deficiency, type 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009876", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009876", 
            "name": "IGHD IA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009876", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009876", 
            "name": "Illig-type growth hormone deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009876", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009876", 
            "name": "congenital isolated GH deficiency type IA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009876", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009876", 
            "name": "non-acquired isolated growth hormone deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009876", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009876", 
            "name": "pituitary dwarfism 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009876", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009876", 
            "name": "congenital IGHD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009876", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009876", 
            "name": "IGHD 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009876", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009876", 
            "name": "IGHD1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009876", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009876", 
            "name": "autosomal recessive isolated growth hormone deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009876", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009876", 
            "name": "pituitary dwarfism I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009876", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009876", 
            "name": "congenital isolated growth hormone deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009876", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009876", 
            "name": "isolated growth hormone deficiency, type IA; IGHD1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009876", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009876", 
            "name": "congenital IGHD type IA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009876", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009876", 
            "name": "sexual ateleiotic dwarfism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009876", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009876", 
            "name": "ILLIG type growth hormone deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009876", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009876", 
            "name": "Growth hormone deficiency, isolated, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009876", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009876", 
            "name": "congenital isolated growth hormone deficiency type IA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009876", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009876", 
            "name": "congenital isolated GH deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009876", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009876", 
            "name": "isolated growth hormone deficiency, type IA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009876", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009876", 
            "name": "isolated growth hormone deficiency type 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009876", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009876", 
            "name": "primordial dwarfism"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060873", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060873", 
            "name": "IGHD IA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060873", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060873", 
            "name": "Illig-type growth hormone deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060873", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060873", 
            "name": "pituitary dwarfism I"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060873", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060873", 
            "name": "primordial dwarfism"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060873", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060873", 
            "name": "sexual ateleiotic dwarfism"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060873", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060873", 
            "name": "autosomal recessive isolated growth hormone deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060873", 
        "description": "An isolated growth hormone deficiency characterized by autosomal recessive inheritance of severe dwarfism with onset by 6 months of age and variable development of antibodies to growth hormone following exogenous supplementation that has material_basis_in null mutations in the GH1 gene on chromosome 17q23.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060873", 
        "name": "isolated growth hormone deficiency type IA"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060873#disease-associations", 
            "id": "0060873", 
            "database": "Alliance of Genome Resources"
        }
    ]
}