Monarch Disease Ontology entry MONDO_0010007 (microbrachycephaly-ptosis-cleft lip syndrome) is characterized by the association of intellectual deficit, microbrachycephaly, hypotelorism, palpebral ptosis, a thin/long face, cleft lip, and anomalies of the lumbar vertebra, sacrum and pelvis. It has been described in two Brazilian sisters. Transmission appears to be autosomal recessive. Also known as: Richieri Costa-Guion Almeida-Ramos syndrome.