DISEASES

Disease-gene associations mined from literature

Human genes for MLS syndrome

MLS syndrome [DOID:0111875]

A syndrome characterized by linear skin defects and various other congenital anomalies. The classical diagnosis consisted of unilateral or bilateral microphthalmia and/or anophthalmia and linear skin defects but patients with a molecular diagnosis of MLS syndrome may not display eye abnormalities.

Synonyms:  MLS syndrome,  DOID:0111875,  MLS disease,  MLS disorder,  MLS syndromes ...