Feingold syndrome

Feingold syndrome (also called oculodigitoesophagoduodenal syndrome) is a rare autosomal dominant hereditary disorder. It is named after Murray Feingold, an American physician who first described the syndrome in 1975. [Source: Wikipedia ]

Synonyms
Microcephaly-mesobrachyphalangy-tracheoesophageal fistula syndrome
Microcephaly-oculo-digito-esophageal-duodenal syndrome
MMT syndrome
MODED syndrome
Oculo-digito-esophagoduodenal syndrome
ODED syndrome
OrphaNet reference
Feingold syndrome 
May Cause
Absent thumb
Anorectal anomaly
Brachydactyly
Clinodactyly
Congenital heart disease
Deafness
Esophageal atresia
Hypoplastic thumb
Microcephaly
Short thumb
Syndactyly
Tracheoesophageal fistula
Vertebral anomaly