Non-Syndromic Syndactyly
Watchlist
Retrieved
2021-01-23
Source
Trials
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Genes
HOXD13,
LRP4,
ABL1,
FZD4,
TFAP2A,
NEDD4L,
JAG2,
FAM92A,
CACNA1C,
FGFR1,
PIK3CA,
ROR2,
LMBR1,
TP63,
CREBBP,
IFT43,
CHSY1,
ANKRD11,
ZDHHC24,
IFT81,
H19,
CCDC22,
TCTN3,
FAM149B1,
CILK1,
HEPHL1,
TMEM216,
MAN1B1,
MED12,
WASHC5
HOXD13,
LRP4,
ABL1,
FZD4,
TFAP2A,
NEDD4L,
JAG2,
FAM92A,
CACNA1C,
FGFR1,
PIK3CA,
ROR2,
LMBR1,
TP63,
CREBBP,
IFT43,
CHSY1,
ANKRD11,
ZDHHC24,
IFT81,
H19,
CCDC22,
TCTN3,
FAM149B1,
CILK1,
HEPHL1,
TMEM216,
MAN1B1,
MED12,
WASHC5,
FIG4,
KIAA0753,
PTDSS1,
BBS1,
KIF7,
NOG,
SLC25A24,
RIPK4,
TXNDC15,
SALL4,
PALB2,
FAT4,
CCDC28B,
BBS5,
CPLANE1,
B3GLCT,
ZSWIM6,
WDR35,
VAC14,
DLL4,
CHD7,
YY1AP1,
CACNA1G,
PHIP,
ESCO2,
MKS1,
ASXL1,
BCOR,
WDR60,
CRIPT,
FGD1,
IGF2,
DHODH,
DSP,
EP300,
DCHS1,
MMUT,
FBN1,
CHRNG,
MYCN,
NOTCH1,
PDE6D,
PRKD1,
CDH3,
HOXA11,
SMO,
FLNA,
TULP1,
BLM,
BBS4,
MKKS,
FGFR2,
NAA10,
OFD1,
LMNA,
GLI3,
SOST,
BHLHA9,
FRAS1,
ZRS,
MSX2,
BMPR1B,
GJA1,
BMP2,
NECTIN4,
GDF5,
CDAN1,
ACSL3,
CKAP2L,
BMP4,
ZNF804A,
MSSD,
FBLN1,
ZNF385B,
CCN6,
FBN2,
FGFR3,
WNT5A,
UVRAG,
TWIST1,
CKAP4,
TCF12,
RPE65,
NECTIN1,
AGO2,
VSX1,
ABHD5,
PHF21A,
MSX1,
MID1,
HPD,
AKIRIN2,
HOXD12,
CUP2Q35,
ALX4,
SMOC1,
HOXD10
Drugs
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Registered!
A group of rare, congenital, non-syndromic distal limb malformation disorders characterized by webbing or fusion of the fingers or toes, involving soft parts only or including bone structure. The morphological anomaly can be unilateral or bilateral, symmetrical or asymmetrical, depending on the specific type.