{"diseases":[{"id":"ORPHA:277","name":"T-B-NK- severe combined immunodeficiency due to adenosine deaminase deficiency","mondoId":"MONDO:0007064","description":null},{"id":"OMIM:274700","name":"Thyroid dyshormonogenesis 3","mondoId":"MONDO:0010135","description":null},{"id":"OMIM:274300","name":"Thyroid hormone resistance, generalized, autosomal recessive","mondoId":"MONDO:0010131","description":null},{"id":"OMIM:618048","name":"Proteasome-Associated autoinflammatory syndrome 2","mondoId":"MONDO:0054700","description":null},{"id":"OMIM:620931","name":"Immunodeficiency 126","mondoId":"MONDO:0975761","description":null},{"id":"OMIM:618534","name":"Immunodeficiency 64","mondoId":"MONDO:0032803","description":null},{"id":"OMIM:621235","name":"Autoimmune disease, multisystem, infantile-onset, 5 ","mondoId":"MONDO:0979235","description":null},{"id":"OMIM:615577","name":"Immunodeficiency, common variable, 10","mondoId":"MONDO:0014260","description":null},{"id":"ORPHA:525731","name":"Pediatric-onset Graves disease","mondoId":"MONDO:0033925","description":null},{"id":"ORPHA:49041","name":"IgG4-related retroperitoneal fibrosis","mondoId":"MONDO:0018848","description":null},{"id":"ORPHA:95715","name":"Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies","mondoId":"MONDO:0019857","description":null},{"id":"OMIM:610199","name":"Diabetes mellitus, neonatal, with congenital hypothyroidism","mondoId":"MONDO:0012436","description":null},{"id":"ORPHA:37042","name":"Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome","mondoId":"MONDO:0010580","description":null},{"id":"OMIM:621096","name":"Immunodeficiency 132B","mondoId":"MONDO:0976228","description":null},{"id":"ORPHA:228426","name":"Syndromic multisystem autoimmune disease due to Itch deficiency","mondoId":"MONDO:0013245","description":null},{"id":"OMIM:620376","name":"Autoinflammatory disease, systemic, with vasculitis","mondoId":"MONDO:0957271","description":null},{"id":"OMIM:301109","name":"Autoinflammatory disease, multisystem, with immune dysregulation, X-linked","mondoId":"MONDO:0957494","description":null},{"id":"ORPHA:566243","name":"Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta","mondoId":"MONDO:0700478","description":null},{"id":"OMIM:621010","name":"Morimoto-Ryu-Malicdan neuromuscular syndrome","mondoId":"MONDO:0975848","description":null},{"id":"ORPHA:95719","name":"Thyroid hemiagenesis","mondoId":"MONDO:0019860","description":null},{"id":"OMIM:609152","name":"Hyperthyroidism, nonautoimmune","mondoId":"MONDO:0012203","description":null},{"id":"OMIM:240300","name":"Autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia","mondoId":"MONDO:0009411","description":null},{"id":"ORPHA:64744","name":"IgG4-related thyroid disease","mondoId":"MONDO:0018992","description":null},{"id":"OMIM:621507","name":"Microcephaly 31, primary, autosomal recessive","mondoId":"MONDO:0980991","description":null},{"id":"ORPHA:3002","name":"Immune thrombocytopenia","mondoId":"MONDO:0008558","description":null}],"genes":[{"id":"NCBIGene:100","name":"ADA"},{"id":"NCBIGene:7038","name":"TG"},{"id":"NCBIGene:7068","name":"THRB"},{"id":"NCBIGene:51371","name":"POMP"},{"id":"NCBIGene:171558","name":"PTCRA"},{"id":"NCBIGene:10125","name":"RASGRP1"},{"id":"NCBIGene:29126","name":"CD274"},{"id":"NCBIGene:4791","name":"NFKB2"},{"id":"NCBIGene:169792","name":"GLIS3"},{"id":"NCBIGene:50943","name":"FOXP3"},{"id":"NCBIGene:7187","name":"TRAF3"},{"id":"NCBIGene:83737","name":"ITCH"},{"id":"NCBIGene:4067","name":"LYN"},{"id":"NCBIGene:139818","name":"DOCK11"},{"id":"NCBIGene:5984","name":"RFC4"},{"id":"NCBIGene:7253","name":"TSHR"},{"id":"NCBIGene:326","name":"AIRE"},{"id":"NCBIGene:1019","name":"CDK4"},{"id":"NCBIGene:9103","name":"FCGR2C"}],"assays":[],"medicalActions":[]}