3-M syndrome (MONDO_0007477, a Monarch Disease Ontology id) can be described as follows. 3M syndrome is a primordial growth disorder characterized by low birth weight, reduced birth length, severe postnatal growth restriction, a spectrum of minor anomalies (including facial dysmorphism) and normal intelligence. Also known as: Dolichospondylic dysplasia, Le Merrer syndrome, Miller-McKusick-Malvaux syndrome, Three M Syndrome, Yakut short stature syndrome, dolichospondylic dysplasia, gloomy face syndrome, three M syndrome.