Disease-gene associations mined from literature

Human genes for Van Maldergem syndrome

Van Maldergem syndrome [DOID:0060238]

A syndrome characterized by facial abnormalities such as telecanthus, epicanthus, broad flattened nose, large inverted W-shaped mouth and malformed ears, malformed extremities such as camptodactyly, clinodactyly, interdigital webbing and joint hyperlaxity and mental retardation.

Synonyms:  Van Maldergem syndrome,  DOID:0060238,  Van Maldergem disease,  Van Maldergem disorder,  Van Maldergem syndromes ...