Term Name: split hand-foot malformation 6
Synonyms: SHFM6
Definition: A split-hand/foot malformation that has_material_basis_in homozygous mutation in the WNT10B gene on chromosome 12q13.
Ontology: Human Disease [DOID:0090026]   ( DOID:0090026 )

Relationships
is a type of: autosomal recessive disease split hand-foot malformation