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 ...