Robinow syndrome

Disease Term Disease ID Gene Symbol Classification References Source
Autosomal dominant Robinow syndrome 3107 DVL1 Causal Pathogenic evidence from ClinVar - ClinVar
DVL3 Causal Pathogenic evidence from ClinVar - ClinVar
FZD2 Causal Pathogenic evidence from ClinVar - ClinVar
WNT5A Causal Pathogenic evidence from ClinVar - ClinVar
Robinow Syndrome C0265205 DVL1 Causal Pathogenic evidence from ClinVar 25817016 ClinVar
DVL3 Causal Pathogenic evidence from ClinVar 26924530 ClinVar
FZD2 Causal Pathogenic evidence from ClinVar 25759469, 29276006 ClinVar
WNT5A Causal Pathogenic evidence from ClinVar 19918918, 24716670 ClinVar
Robinow Syndrome, Autosomal Dominant C4551476 DVL1 Causal Pathogenic evidence from ClinVar - ClinVar
DVL3 Causal Pathogenic evidence from ClinVar - ClinVar
ROR2 Causal Pathogenic evidence from ClinVar - ClinVar
WNT5A Causal Pathogenic evidence from ClinVar - ClinVar
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2 C4225363 DVL1 Causal Pathogenic evidence from ClinVar 25817014, 25817016, 26924530, 29276006 ClinVar
DVL3 Causal Pathogenic evidence from ClinVar - ClinVar
FZD2 Causal Pathogenic evidence from ClinVar - ClinVar
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1 C4551475 DVL3 Causal Pathogenic evidence from ClinVar 26924530 ClinVar
ROR2 Causal Pathogenic evidence from ClinVar 19461659 ClinVar
WNT5A Causal Pathogenic evidence from ClinVar 19918918 ClinVar
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3 C4225164 DVL3 Causal Pathogenic evidence from ClinVar 26924530, 29575616 ClinVar
FZD2 Causal Pathogenic evidence from ClinVar - ClinVar
Autosomal recessive Robinow syndrome 1507 NXN Causal Pathogenic evidence from ClinVar - ClinVar
ROR2 Causal Pathogenic evidence from ClinVar - ClinVar
Robinow syndrome, autosomal recessive C1849334 NXN Causal Pathogenic evidence from ClinVar 29276006 ClinVar
ROR2 Causal Pathogenic evidence from ClinVar 10932186, 10932187, 12815588, 15952209, 19461659, 19640924 ClinVar