has material basis in germline mutation in STRA6 Matthew-Wood syndrome https://www.malacards.org/card/microphthalmia_syndromic_9_2 Matthew Wood syndrome microphthalmia syndromic type 9 Orphanet:2470 GARD:0000713 clinical anophthalmia mild facial dysmorphism lung heart and diaphragm malformations Matthew-Wood syndrome OMIM:601186 Matthew-Wood syndrome is a rare clinical entity including as main characteristics anophthalmia or severe microphthalmia, and pulmonary hypoplasia or aplasia. DOID:0050819 MCOPS9 microphthalmia syndromic 9 MONDO:0011010 MEDGEN:318679 UMLS:C1832661 anophthalmia-pulmonary hypoplasia syndrome pulmonary agenesis microphthalmi and diaphragmatic defect syndromic microphthalmia type 9 microphthalmia, syndromic type 9 DOID:0111807 MESH:C537768 microphthalmia, syndromic 9 SCTID:722458000 multiple congenital anomalies/dysmorphic syndrome without intellectual disability obsolete non-syndromic respiratory or mediastinal malformation thoracic malformation syndromic microphthalmia