Details for Disease 442

DISEASE NAME Congenital hypothyroidism
DISEASE CATEGORY (ICD10) None
DISEASE ID (ICD10) E00.9
DISEASE ID (OMIM) N.A.
118 combinations linked to 442 OLI031; OLI032; OLI040; OLI464; OLI465; OLI466; OLI467; OLI468; OLI469; OLI470; OLI471; OLI472; OLI473; OLI474; OLI518; OLI519; OLI520; OLI562; OLI563; OLI564; OLI565; OLI566; OLI567; OLI580; OLI581; OLI582; OLI583; OLI584; OLI585; OLI586; OLI587; OLI588; OLI589; OLI590; OLI591; OLI592; OLI593; OLI594; OLI595; OLI596; OLI986; OLI987; OLI988; OLI989; OLI990; OLI991; OLI992; OLI993; OLI994; OLI995; OLI1020; OLI1021; OLI1022; OLI1023; OLI1024; OLI1025; OLI1026; OLI1073; OLI1074; OLI1075; OLI1076; OLI1077; OLI1078; OLI1079; OLI1080; OLI1081; OLI1082; OLI1083; OLI1084; OLI1085; OLI1086; OLI1087; OLI1088; OLI1089; OLI1090; OLI1091; OLI1092; OLI1093; OLI1094; OLI1173; OLI1174; OLI1175; OLI1481; OLI1482; OLI1483; OLI1484; OLI1485; OLI1486; OLI1487; OLI1488; OLI1489; OLI1490; OLI1491; OLI1492; OLI1493; OLI1494; OLI1495; OLI1496; OLI1497; OLI1498; OLI1499; OLI1500; OLI1501; OLI1502; OLI1503; OLI1504; OLI1505; OLI1506; OLI1507; OLI1607; OLI1608; OLI1609; OLI1804; OLI1805; OLI1806; OLI1807; OLI1808; OLI1809
59 gene combinations linked to 442 NKX2-1; TG; JAG1; TSHR; GLIS3; JAG1; NKX2-1; DUOX2; GLIS3; JAG1; TG; GLIS3; SLC26A4; TSHR; SLC26A4; TPO; TSHR; JAG1; NKX2-1; FOXE1; TSHR; DUOX2; PAX8; SLC26A4; GLIS3; PAX8; DUOX2; TPO; GLIS3; SLC26A4; SLC26A4; TG; DUOX2; DUOXA1; FOXE1; DUOX2; DUOXA2; GLIS3; SHH; DUOX2; SHH; HOXB3; SLC26A4; SLC26A4; TSHR; DUOX2; TG; TPO; DUOX1; DUOX2; DUOX2; DUOXA1; GLIS3; DUOX2; DUOXA1; JAG1; DUOXA1; JAG1; CDCA8; DUOX2; DUOX2; NKX2-1; TSHR; DUOX2; NKX2-1; TG; DUOX2; SHH; TG; CDCA8; SHH; SLC26A4; HOXB3; TG; DUOX2; HOXB3; DUOX2; EYA1; EYA1; TG; DUOXA2; HES1; TPO; NKX2-5; TG; GNAS; PAX8; TG; HOXB3; JAG1; TG; EYA1; TPO; DUOX2; PSMD2; DUOXA2; TBX1; SLC26A4; TRHR; DUOX2; SLC26A4; DUOXA2; TG; DUOX2; TG; TG; TPO; DUOX2; DUOXA2; TG; TPO; TSHR; GLIS3; TPO; SLC26A4; TPO; DUOXA2; TPO; TSHR; DUOX2; TSHR; TG; TSHR; KMT2D; TPO; KMT2D; TG; URB1; KMT2D; NKX2-5; TG; HOXB3; HOXD3; DUOX2; DUOXA2; DUOXA2; SLC26A4; TG; IGSF1; TG
ORPHANET ID 442
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