Renal Agenesis, Bilateral
Watchlist
Retrieved
2021-01-23
Source
Trials
—
Genes
RET,
ITGA8,
GREB1L,
FREM1,
FGF20,
ANOS1,
FREM2,
SIX1,
DHCR7,
CCDC141,
PUF60,
PHGDH,
TCTN3,
KIF7,
NSMF,
SH2B1,
NDUFAF3,
FLRT3,
CIT,
NSDHL,
SDCCAG8,
SEMA3A,
SCO2,
KIF14,
KIAA0753,
SEMA3E,
HS6ST1,
FOXH1,
FGF17,
DLL1
RET,
ITGA8,
GREB1L,
FREM1,
FGF20,
ANOS1,
FREM2,
SIX1,
DHCR7,
CCDC141,
PUF60,
PHGDH,
TCTN3,
KIF7,
NSMF,
SH2B1,
NDUFAF3,
FLRT3,
CIT,
NSDHL,
SDCCAG8,
SEMA3A,
SCO2,
KIF14,
KIAA0753,
SEMA3E,
HS6ST1,
FOXH1,
FGF17,
DLL1,
CDON,
FAM149B1,
PIEZO2,
PROKR2,
CCNQ,
DISP1,
KISS1R,
SPRY4,
VANGL1,
FUZ,
THOC6,
CPLANE1,
PROK2,
TMEM216,
SALL4,
WDR11,
CHD7,
CEP55,
MKS1,
IL17RD,
WNT4,
ATRX,
SUFU,
HESX1,
FEZF1,
TP63,
NDUFS2,
LRP4,
OFD1,
HOXD13,
HNF4A,
GLI3,
GLI2,
GAS1,
FGFR2,
FGFR3,
FGFR1,
FGF10,
FGF8,
FANCB,
FANCE,
FANCD2,
FANCC,
FANCA,
EYA1,
DUSP6,
DHCR24,
DCC,
NDUFB8,
INSL3,
NODAL,
SIX3,
ZIC3,
ZIC2,
WNT3,
TGIF1,
TFAP2A,
TDGF1,
HNF1B,
TACR3,
SOX10,
SURF1,
PTCH1,
PBX1,
RPL26,
PDE6D,
SHH,
FRAS1,
HOXD11,
CFTR,
GEN1,
IFNG,
SOX9,
NOTUM,
RARA,
GDNF,
RAB40B,
IFT27,
SOX8,
AFP
Drugs
—
Registered!
A form of renal agenesis characterized by complete absence of kidney development, absent ureters and subsequent absence of fetal renal function resulting in Potter sequence with pulmonary hypoplasia related to oligohydramnios, which is fatal shortly after birth.