cutaneous finger syndactyly Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A soft tissue continuity in the A/P axis between two fingers that extends distally to at least the level of the proximal interphalangeal joints, or a soft tissue continuity in the A/P axis between two fingers that lies significantly distal to the flexion crease that overlies the metacarpophalangeal joint of the adjacent fingers. (Human Phenotype Ontology, HP_0010554)
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21 genes associated with the cutaneous finger syndactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CCBE1 collagen and calcium binding EGF domains 1
DCHS1 dachsous cadherin-related 1
FAT4 FAT atypical cadherin 4
FGFR2 fibroblast growth factor receptor 2
FRAS1 Fraser extracellular matrix complex subunit 1
FREM2 FRAS1 related extracellular matrix protein 2
GRIP1 glutamate receptor interacting protein 1
HOXD13 homeobox D13
IRF6 interferon regulatory factor 6
KCTD1 potassium channel tetramerization domain containing 1
LMBR1 limb development membrane protein 1
LRP4 low density lipoprotein receptor-related protein 4
MEGF8 multiple EGF-like-domains 8
NOG noggin
ORC1 origin recognition complex, subunit 1
PAX3 paired box 3
PIEZO2 piezo-type mechanosensitive ion channel component 2
PVRL1 poliovirus receptor-related 1 (herpesvirus entry mediator C)
PVRL4 poliovirus receptor-related 4
ROR2 receptor tyrosine kinase-like orphan receptor 2
WDR19 WD repeat domain 19