{
    "disease_id": "DOID:0060873",
    "recommended_name": {
        "id": "DOID:0060873",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060873",
        "name": "isolated growth hormone deficiency type IA",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0060873",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060873",
            "name": "IGHD IA",
            "description": ""
        },
        {
            "id": "DOID:0060873",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060873",
            "name": "Illig-type growth hormone deficiency",
            "description": ""
        },
        {
            "id": "DOID:0060873",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060873",
            "name": "pituitary dwarfism I",
            "description": ""
        },
        {
            "id": "DOID:0060873",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060873",
            "name": "primordial dwarfism",
            "description": ""
        },
        {
            "id": "DOID:0060873",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060873",
            "name": "sexual ateleiotic dwarfism",
            "description": ""
        },
        {
            "id": "DOID:0060873",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060873",
            "name": "autosomal recessive isolated growth hormone deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009876",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009876",
            "name": "isolated growth hormone deficiency type IA",
            "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."
        },
        {
            "id": "MONDO:0009876",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009876",
            "name": "Illig-type growth hormone deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009876",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009876",
            "name": "congenital IGHD type IA",
            "description": ""
        },
        {
            "id": "MONDO:0009876",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009876",
            "name": "congenital isolated GH deficiency type IA",
            "description": ""
        },
        {
            "id": "MONDO:0009876",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009876",
            "name": "congenital isolated growth hormone deficiency type IA",
            "description": ""
        },
        {
            "id": "MONDO:0009876",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009876",
            "name": "growth hormone deficiency, isolated, type IA",
            "description": ""
        },
        {
            "id": "MONDO:0009876",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009876",
            "name": "isolated growth hormone deficiency type IA",
            "description": ""
        },
        {
            "id": "MONDO:0009876",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009876",
            "name": "primordial dwarfism",
            "description": ""
        },
        {
            "id": "MONDO:0009876",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009876",
            "name": "sexual ateleiotic dwarfism",
            "description": ""
        },
        {
            "id": "MONDO:0009876",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009876",
            "name": "Growth hormone deficiency, isolated autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0009876",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009876",
            "name": "IGHD1A",
            "description": ""
        },
        {
            "id": "MONDO:0009876",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009876",
            "name": "ILLIG type growth hormone deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009876",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009876",
            "name": "congenital IGHD",
            "description": ""
        },
        {
            "id": "MONDO:0009876",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009876",
            "name": "congenital isolated GH deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009876",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009876",
            "name": "congenital isolated growth hormone deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009876",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009876",
            "name": "isolated growth hormone deficiency type 1A",
            "description": ""
        },
        {
            "id": "MONDO:0009876",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009876",
            "name": "isolated growth hormone deficiency, type IA",
            "description": ""
        },
        {
            "id": "MONDO:0009876",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009876",
            "name": "non-acquired isolated growth hormone deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009876",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009876",
            "name": "pituitary dwarfism 1",
            "description": ""
        },
        {
            "id": "MIM:262400",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/262400",
            "name": "Growth hormone deficiency, isolated, 1A",
            "description": "Growth hormone deficiency, isolated, 1A"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060873"
    ],
    "unlinked_id_list": []
}