Monarch Disease Ontology identifier MONDO_0014096 (microcephaly-intellectual disability-phalangeal and neurological anomalies syndrome) can be described as follows. This syndrome is characterized by microcephaly, severe intellectual deficit, phalangeal anomalies (cutaneous syndactyly of the fingers, toe brachyclinodactyly and nail hypoplasia) and neurological manifestations (epilepsy, spastic/dystonic paraplegia and brisk reflexes). Also known as: Woods-Crouchman-Huson syndrome.