{
    "disease_id": "DOID:0081046",
    "recommended_name": {
        "id": "DOID:0081046",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081046",
        "name": "frontonasal dysplasia 2",
        "description": "A frontonasal dysplasia that has_material_basis_in homozygous mutation in the ALX4 gene on chromosome 11p11."
    },
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            "id": "MONDO:0013268",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013268",
            "name": "frontonasal dysplasia with alopecia and genital anomaly",
            "description": "Frontonasal dysplasia with alopecia and genital anomaly is a new phenotype of frontonasal dysplasia associated with total alopecia and hypogonadism."
        },
        {
            "id": "MONDO:0013268",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013268",
            "name": "ALX4-related FNDAG",
            "description": ""
        },
        {
            "id": "MONDO:0013268",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013268",
            "name": "craniofrontonasal dysplasia with alopecia and hypogonadism",
            "description": ""
        },
        {
            "id": "MONDO:0013268",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013268",
            "name": "frontonasal dysplasia type 2",
            "description": ""
        },
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            "resource": "MONDO",
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            "name": "frontonasal dysplasia with alopecia and genital abnomality",
            "description": ""
        },
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            "resource": "MONDO",
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            "name": "FND2",
            "description": ""
        },
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            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013268",
            "name": "frontonasal dysplasia 2",
            "description": ""
        },
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            "url": "https://www.omim.org/entry/613451",
            "name": "Frontonasal dysplasia 2",
            "description": "Frontonasal dysplasia 2"
        }
    ],
    "children": [],
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    ],
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            "url": "https://disease-ontology.org/term/DOID:0081046",
            "categories": []
        },
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            "url": "https://monarchinitiative.org/disease/MONDO:0013268",
            "categories": []
        },
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            "categories": []
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            "uniprot_ac": "E7FGP3",
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                    "glygen_name": "Zebrafish",
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            ],
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                },
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            ],
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                    "name": "alx4a",
                    "type": "recommended"
                },
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                    "name": "Homo sapiens",
                    "taxid": 9606,
                    "common_name": "Human",
                    "glygen_name": "Human",
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                {
                    "name": "homeobox protein aristaless-like 4",
                    "type": "synonym"
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                    "name": "homeodomain transcription factor ALX4",
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                    "type": "recommended"
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                    "type": "synonym"
                },
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                    "name": "CRS5",
                    "type": "synonym"
                },
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                    "name": "FND2",
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                },
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                    "name": "KIAA1788",
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            "species": [
                {
                    "name": "Rattus norvegicus",
                    "taxid": 10116,
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}