Hernia, Anterior Diaphragmatic
Watchlist
Retrieved
2019-09-22
Source
Trials
—
Genes
GATA4,
ZFPM2,
WT1,
GATA6,
STAT3,
FREM1,
KCNQ5,
FGFRL1,
CCL2,
EPO,
FOXC2,
DES,
IGF2R,
MYOD1,
FOXF1,
IGF1R,
RHOA,
PIM1,
INSR,
WNT11,
CCN2,
EFNB1,
PIGN,
RARB,
FBN1,
LRP2,
GPC3,
NIPBL,
MYRF,
FREM2
GATA4,
ZFPM2,
WT1,
GATA6,
STAT3,
FREM1,
KCNQ5,
FGFRL1,
CCL2,
EPO,
FOXC2,
DES,
IGF2R,
MYOD1,
FOXF1,
IGF1R,
RHOA,
PIM1,
INSR,
WNT11,
CCN2,
EFNB1,
PIGN,
RARB,
FBN1,
LRP2,
GPC3,
NIPBL,
MYRF,
FREM2,
FRAS1,
ARID1A,
TRRAP,
SMC1A,
SMC3,
HOXD13,
KMT2D,
HCCS,
HDAC4,
KIAA0586,
POGZ,
NELFA,
KCNA1,
DPF2,
RAP1B,
RAP1A,
RAD21,
PMM2,
ABL1,
PBX1,
SMARCA4,
SMARCB1,
SMARCC2,
SMARCE1,
SOX4,
KMT2A,
SOX11,
TRPS1,
LFNG,
CD96,
KDM6A,
NSD2,
LETM1,
RPS28,
GLI3,
DIS3L2,
HDAC8,
DHCR7,
ARID1B,
TRAIP,
ARID2,
MESP2,
STRA6,
COX7B,
PORCN,
CHRNG,
CDK8,
SLC2A10,
UTP23,
HES7,
RIPPLY2,
MCTP2,
PGAP3,
RSPO2,
DLL3,
SETD5,
FBLN5,
NDUFB11,
ROBO4,
WNT4,
SUFU,
KIF7,
DACT1,
EFEMP2,
SH2B1,
SIN3A,
GPC4,
FLNA,
NR2F2,
HTC2,
VEGFA,
MIR200B,
NAT2,
CYP2E1,
CHDH,
TGFB2,
EDN1,
ACTB,
EDNRB,
DISP1,
SFTPC,
SFTPB,
TNF,
SLIT3,
MEF2A,
IL10,
CRP,
RPS19,
PCNA,
EDNRA,
CD44,
ACTA2,
LHCGR,
BMPR2,
EPAS1,
HLX,
GSTM1,
ELN,
DIH1,
DMRT1,
SDHA,
ASAH2,
RGMA,
PJA1,
ACE,
EFNB2,
DRD4,
ECE1,
CHD2,
EGF,
ELF3,
ENG,
NOSIP,
EPHB4,
IGHV1-12,
CHMP2B,
ERN1,
ESR1,
FGF7,
COL1A1,
CRISPLD2,
CDH15,
NEIL2,
TLX1NB,
SFTPA2,
SFTPA1,
PLF,
MIR33A,
MIR130A,
MIRLET7B,
AFP,
GSTK1,
AGER,
AGT,
PIGW,
AGTR1,
SOX7,
AKT1,
ANGPT1,
AQP6,
SLCO6A1,
XIRP2,
EGLN3,
CASR,
DSEL,
ARRDC4,
CAV1,
CD79A,
FOXC1,
FGF10,
FZD2,
MTOR,
TBX5,
TRPC6,
LLGL1,
TM7SF2,
TIMP2,
SMAD2,
TGFA,
NR2F1,
TF,
TEK,
TCTE3,
TCF7L2,
TCF4,
TBX2,
FSTL1,
TBX1,
MIF,
SPP1,
MKI67,
MMP2,
MYL2,
NFATC2,
NOS3,
SLC11A2,
SLC6A3,
SFTPD,
RAC1,
TRV-CAC1-2,
TWIST1,
UROD,
LEP,
EMILIN1,
GFER,
TUBA1B,
GJB2,
GPI,
EDIL3,
ZEB2,
NR3C1,
STARD8,
TBX4,
KCNQ4,
NRG1,
ALDH1A2,
FGF18,
ITGA8,
AXIN2,
FOXA2,
HOXB9,
GDF5,
NDST1,
NR4A3,
IL4,
ITGA6,
KIF22,
LCN2,
MIR1307
Drugs
Registered!
Lilly et al. (1974) described a family in which 2 brothers and their maternal uncle had congenital, anterior diaphragmatic hernia. Two of the 3 died in infancy of complications. Crane (1979) favored multifactorial inheritance with high male:female sex ratio. Twelve multiplex families were analyzed.