Details for Disease 168778

DISEASE NAME Rare pervasive developmental disorder
DISEASE CATEGORY (ICD10) Mental and behavioural disorders
DISEASE ID (ICD10) F84.8
DISEASE ID (OMIM) N.A.
40 combinations linked to 168778 OLI432; OLI433; OLI434; OLI475; OLI476; OLI477; OLI478; OLI479; OLI480; OLI481; OLI482; OLI483; OLI484; OLI485; OLI486; OLI487; OLI488; OLI489; OLI490; OLI491; OLI492; OLI493; OLI494; OLI495; OLI496; OLI932; OLI1460; OLI1461; OLI1462; OLI1463; OLI1464; OLI1465; OLI1466; OLI1467; OLI1468; OLI1469; OLI1706; OLI1707; OLI1709; OLI1710
37 gene combinations linked to 168778 CACNA1H; RELN; CACNA2D4; VLDLR; RELN; RYR3; RELN; RYR2; ELP4; RELN; RYR1; ORAI1; RELN; CACNA1B; VLDLR; GRIN2C; KDM6B; RELN; CACNA1H; CACNA2D4; RELN; CACNA1A; CACNB2; RELN; EHMT1; SLC9A6; EHMT1; MFSD8; MTHFR; SCN2A; ALDH5A1; ATG7; DIP2C; HUWE1; ITPR3; TPH2; DEAF1; EPHA5; CLCN3; LRIF1; KMT2C; KMT5A; DHX30; LRRC18; PARP14; PDPR; HOXA1; TSC2; CACNA1C; SHANK3; HOXA1; UBE3A; HOXA1; TSC1; TSC1; UBE3A; CACNA1C; TSC2; CACNA1C; CDKL5; CACNA1C; TSC1; TSC1; TSC2; CACNA1C; FOXP2; FOXP2; GRID2; GRID2; TSC1; CACNA1C; EML1; TSC1; SHANK3; TSC1; CACNA1C; MECP2; CACNA1C; HOXA1; CACNA1C; GRID2; SHANK3; UBE3A; TSC2; UBE3A
ORPHANET ID 168778
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