microphthalmia, syndromic 9 https://github.com/monarch-initiative/mondo/issues/10151 https://www.malacards.org/card/microphthalmia_syndromic_9_2 Spear syndrome Orphanet:2470 GARD:0000713 pulmonary agenesis microphthalmi and diaphragmatic defect STRA6-related syndromic microphthalmia Matthew-Wood syndrome A syndromic microphthalmiae in which the cause of the disease is a mutation in the STRA6 gene. It is characterized by microphthalmia or anophthalmia, and variable features including including intellectual disability, pulmonary hypoplasia or agenesis, congenital diaphragmatic hernia or eventration and congenital heart disease. OMIM:601186 Matthew Wood syndrome DOID:0050819 clinical anophthalmia mild facial dysmorphism lung heart and diaphragm malformations MCOPS9 MONDO:0011010 MEDGEN:318679 UMLS:C1832661 anophthalmia-pulmonary hypoplasia syndrome microphthalmia syndromic 9 DOID:0111807 MESH:C537768 SCTID:722458000 multiple congenital anomalies/dysmorphic syndrome without intellectual disability obsolete non-syndromic respiratory or mediastinal malformation thoracic malformation syndromic microphthalmia obsolete_Matthew-Wood syndrome