Human genes for Fuhrmann syndrome
Fuhrmann syndrome [DOID:0090067]
A bone development disease that is characterized by bowing of the femora, aplasia or hypoplasia of the fibulae and poly-, oligo-, and syndactyly that has_material_basis_in autosomal recessive inheritance of homozygous mutation in the Wnt family member 7A (WNT7A) gene on chromosome 3p25.
Synonyms: Fuhrmann syndrome, DOID:0090067, Fuhrmann disease, Fuhrmann disorder, Fuhrmann syndromes