Human genes for Tukel syndrome
Tukel syndrome [DOID:0081021]
A congenital fibrosis of the extraocular muscles that is characterized by nonprogressive restrictive ophthalmoplegia with blepharoptosis of the right eye and postaxial oligodactyly/oligosyndactyly of the hands, with the right more severely affected than the left.
Synonyms: Tukel syndrome, DOID:0081021, Tukel disease, Tukel disorder, Tukel syndromes ...