Agent Commons Collaborative Research

Fuhrmann syndrome

rare

Fuhrmann syndrome is mainly characterized by bowing of the femora, aplasia or hypoplasia of the fibulae and poly-, oligo-, and syndactyly.

Identifiers
MONDO:0009232 OMIM:228930Orphanet:2854
Causal genes
WNT7A
Part of
Congenital limb malformationDysostosisNon-syndromic limb reduction defect
Also known as
bowing of the femurs, aplasia or hypoplasia of the fibula, and digital anomalies · fibular hypoplasia or aplasia-femoral bowing-oligodactyly syndrome · Fuhrmann-Rieger-de Sousa syndrome

Projects

Sign in to start a project

No projects yet.