{
    "disease_id": "DOID:0111807",
    "recommended_name": {
        "id": "DOID:0111807",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111807",
        "name": "syndromic microphthalmia 9",
        "description": "A syndromic microphthalmia characterized by bilateral clinical anophthalmia, pulmonary hypoplasia or aplasia, cardiac malformations, and diaphragmatic defects that has_material_basis_in homozygous or compound heterozygous mutation in the STRA6 gene on chromosome 15q24.1."
    },
    "synonyms": [
        {
            "id": "DOID:0111807",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111807",
            "name": "pulmonary agenesis microphthalmi and diaphragmatic defect",
            "description": ""
        },
        {
            "id": "DOID:0111807",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111807",
            "name": "Matthew-Wood syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111807",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111807",
            "name": "anophthalmia-pulmonary hypoplasia syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111807",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111807",
            "name": "spear syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111807",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111807",
            "name": "anophthalmia/microphthalmia and pulmonary hypoplasia",
            "description": ""
        },
        {
            "id": "DOID:0111807",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111807",
            "name": "clinical anophthalmia mild facial dysmorphism lung heart and diaphragm malformations",
            "description": ""
        },
        {
            "id": "MONDO:0011010",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011010",
            "name": "Matthew-Wood syndrome",
            "description": "Matthew-Wood syndrome is a rare clinical entity including as main characteristics anophthalmia or severe microphthalmia, and pulmonary hypoplasia or aplasia."
        },
        {
            "id": "MONDO:0011010",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011010",
            "name": "MCOPS9",
            "description": ""
        },
        {
            "id": "MONDO:0011010",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011010",
            "name": "Matthew-Wood syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011010",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011010",
            "name": "anophthalmia-pulmonary hypoplasia syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011010",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011010",
            "name": "microphthalmia syndromic type 9",
            "description": ""
        },
        {
            "id": "MONDO:0011010",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011010",
            "name": "microphthalmia, syndromic type 9",
            "description": ""
        },
        {
            "id": "MONDO:0011010",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011010",
            "name": "syndromic microphthalmia type 9",
            "description": ""
        },
        {
            "id": "MONDO:0011010",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011010",
            "name": "Matthew Wood syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011010",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011010",
            "name": "clinical anophthalmia mild facial dysmorphism lung heart and diaphragm malformations",
            "description": ""
        },
        {
            "id": "MONDO:0011010",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011010",
            "name": "microphthalmia syndromic 9",
            "description": ""
        },
        {
            "id": "MONDO:0011010",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011010",
            "name": "microphthalmia, syndromic 9",
            "description": ""
        },
        {
            "id": "MONDO:0011010",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011010",
            "name": "pulmonary agenesis microphthalmi and diaphragmatic defect",
            "description": ""
        },
        {
            "id": "MIM:601186",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/601186",
            "name": "Microphthalmia, syndromic, 9",
            "description": "Microphthalmia, syndromic, 9"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111807"
    ],
    "unlinked_id_list": []
}