hereditary disease ophthalmomandibulomelic dysplasia https://www.malacards.org/card/ophthalmomandibulomelic_dysplasia MESH:C563501 Pillay syndrome MONDO:0008127 OMIM:164900 GARD:0004365 UMLS:C1833872 SCTID:715484003 Ophthalmomandibulomelic dysplasia is characterized by complete blindness due to corneal opacities, difficult mastication due to temporomandibular fusion and anomalies of the arms. Ophthalmo-mandibulo-melic dysplasia ophthalmomandibulomelic dysplasia MEDGEN:331604 icd11.foundation:869046719 Orphanet:2741 OMM syndrome obsolete syndromic corneal dystrophy