{
    "disease_id": "DOID:0050545",
    "recommended_name": {
        "id": "DOID:0050545",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0050545",
        "name": "visceral heterotaxy",
        "description": "A physical disorder characterized by the abnormal distribution of the major visceral organs within the chest and abdomen."
    },
    "synonyms": [
        {
            "id": "DOID:0050545",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050545",
            "name": "heterotaxia",
            "description": ""
        },
        {
            "id": "DOID:0050545",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050545",
            "name": "situs ambiguus",
            "description": ""
        },
        {
            "id": "MONDO:0011546",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011546",
            "name": "heterotaxy, visceral, 2, autosomal",
            "description": ""
        },
        {
            "id": "MONDO:0011546",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011546",
            "name": "heterotaxy, visceral, 2, autosomal",
            "description": ""
        },
        {
            "id": "MONDO:0011546",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011546",
            "name": "HTX2",
            "description": ""
        },
        {
            "id": "MONDO:0011546",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011546",
            "name": "heterotaxy, visceral, 2, autosomal; HTX2",
            "description": ""
        },
        {
            "id": "MONDO:0011546",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011546",
            "name": "Htx",
            "description": ""
        },
        {
            "id": "MONDO:0011546",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011546",
            "name": "transposition of the great arteries, dextro-looped 2; DTGA2",
            "description": ""
        },
        {
            "id": "MONDO:0011659",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011659",
            "name": "HTX3",
            "description": ""
        },
        {
            "id": "MONDO:0011659",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011659",
            "name": "HTX3",
            "description": ""
        },
        {
            "id": "MONDO:0011659",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011659",
            "name": "heterotaxy, visceral, 3, autosomal; HTX3",
            "description": ""
        },
        {
            "id": "MONDO:0011659",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011659",
            "name": "heterotaxy, visceral, 3, autosomal",
            "description": ""
        },
        {
            "id": "MONDO:0010607",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010607",
            "name": "heterotaxy, visceral, 1, X-linked",
            "description": "X-linked visceral heterotaxy type 1 is a very rare form of heterotaxy that has only been reported in a few families. Heterotaxy is the right/left transposition of thoracic and/or abdominal organs. This condition is caused by mutations in the ZIC3 gene, is inherited in an X-linked recessive fashion , and is usually seen in males. Physical features include heart abnormalities such as dextrocardia , transposition of great vessels , ventricular septal defect , patent ductus arteriosus , pulmonic stenosis ; situs inversus, and missing (asplenia) and/or extra spleens (polysplenia).Affected individualscan also experience abnormalities in the development of the midline of the body, which can cause holoprosencephaly , myelomeningocele , urological anomalies, widely spaced eyes (hypertelorism), cleft palate , and abnormalities of the sacral spine and anus. Heterotaxia with recurrent respiratory infections are called primary ciliary dyskinesia ."
        },
        {
            "id": "MONDO:0010607",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010607",
            "name": "heterotaxy, visceral, 1, X-linked; HTX1",
            "description": ""
        },
        {
            "id": "MONDO:0010607",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010607",
            "name": "HTX1",
            "description": ""
        },
        {
            "id": "MONDO:0010607",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010607",
            "name": "X-linked visceral heterotaxy 1",
            "description": ""
        },
        {
            "id": "MONDO:0010607",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010607",
            "name": "heterotaxy, visceral, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010607",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010607",
            "name": "laterality, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010607",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010607",
            "name": "dextrocardia with Other Cardiac malformations",
            "description": ""
        },
        {
            "id": "MONDO:0010607",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010607",
            "name": "situs inversus, Complex Cardiac defects, and splenic defects, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010607",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010607",
            "name": "congenital heart defects, multiple types, 1, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010607",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010607",
            "name": "heterotaxy, visceral, 1, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010607",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010607",
            "name": "ZIC3 visceral heterotaxy",
            "description": ""
        },
        {
            "id": "MONDO:0010607",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010607",
            "name": "visceral heterotaxy caused by mutation in ZIC3",
            "description": ""
        },
        {
            "id": "MONDO:0013887",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013887",
            "name": "heterotaxy, visceral, 6, autosomal",
            "description": ""
        },
        {
            "id": "MONDO:0013887",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013887",
            "name": "heterotaxy, visceral, 6, autosomal",
            "description": ""
        },
        {
            "id": "MONDO:0013887",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013887",
            "name": "heterotaxy, visceral, 6, autosomal; HTX6",
            "description": ""
        },
        {
            "id": "MONDO:0013887",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013887",
            "name": "HTX6",
            "description": ""
        },
        {
            "id": "MONDO:0013403",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013403",
            "name": "heterotaxy, visceral, 4, autosomal",
            "description": "Any visceral heterotaxy in which the cause of the disease is a mutation in the ACVR2B gene."
        },
        {
            "id": "MONDO:0013403",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013403",
            "name": "HTX4",
            "description": ""
        },
        {
            "id": "MONDO:0013403",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013403",
            "name": "heterotaxy, visceral, 4, autosomal",
            "description": ""
        },
        {
            "id": "MONDO:0013403",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013403",
            "name": "ACVR2B visceral heterotaxy",
            "description": ""
        },
        {
            "id": "MONDO:0013403",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013403",
            "name": "heterotaxy, visceral, 4, autosomal; HTX4",
            "description": ""
        },
        {
            "id": "MONDO:0013403",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013403",
            "name": "visceral heterotaxy caused by mutation in ACVR2B",
            "description": ""
        },
        {
            "id": "MIM:605376",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/605376",
            "name": "Heterotaxy, visceral, 2, autosomal",
            "description": "Heterotaxy, visceral, 2, autosomal"
        },
        {
            "id": "MIM:306955",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/306955",
            "name": "Heterotaxy, visceral, 1, X-linked",
            "description": "Heterotaxy, visceral, 1, X-linked"
        },
        {
            "id": "MIM:614779",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614779",
            "name": "Heterotaxy, visceral, 6, autosomal",
            "description": "Heterotaxy, visceral, 6, autosomal"
        },
        {
            "id": "MIM:613751",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613751",
            "name": "Heterotaxy, visceral, 4, autosomal",
            "description": "Heterotaxy, visceral, 4, autosomal"
        }
    ]
}