Disease-gene associations mined from literature

Human genes for Dubowitz syndrome

Dubowitz syndrome [DOID:14796]

A syndrome that is a rare genetic disorder characterized by microcephaly, growth retardation and a characteristic facial appearance like small, round, triangular shaped with a pointed, receding chin, a broad, wide-tipped nose, and wide-set eyes with drooping eyelids.

Synonyms:  Dubowitz syndrome,  DOID:14796,  Dubowitz disease,  Dubowitz disorder,  Dubowitz syndromes ...

Linkouts:  OMIM