obsolete_2q24 microdeletion syndrome true orphanet ICD10:Q93.5 http://purl.obolibrary.org/obo/MONDO_0015566 UMLS:C2931816 Monosomy 2q24 MESH:C538316 Del(2)(q24) 2q24 microdeletion syndrome is a chromosomal anomaly consisting of a partial long arm deletion of chromosome 2 and characterized clinically by a wide range of manifestations (depending on the specific region deleted) which can include seizures, microcephaly, dysmorphic features, cleft palate, eye abnormalities (coloboma, cataract and microphthalmia), growth retardation, failure to thrive, heart defects, limb anomalies, developmental delay and autism. Replaced with Mondo term. 3.41.0