- OMIM ID
-
164280
- OMIM term:
- FEINGOLD SYNDROME 1; FGLDS1
- Alternative terms:
-
FEINGOLD SYNDROME
OCULODIGITOESOPHAGODUODENAL SYNDROME; ODED
ODED SYNDROME
MICROCEPHALY-OCULO-DIGITO-ESOPHAGEAL-DUODENAL SYNDROME; MODED
DIGITAL ANOMALIES WITH SHORT PALPEBRAL FISSURES AND ATRESIA OF ESOPHAGUS OR DUODENUM
MICROCEPHALY, MENTAL RETARDATION, AND TRACHEOESOPHAGEAL FISTULA SYNDROME
MMT SYNDROME
MICROCEPHALY AND DIGITAL ABNORMALITIES WITH NORMAL INTELLIGENCE
- (∗) Location:
- 2p24.3
- (†) Associated OMIM genes:
- MYCN
- (‡) Associated MGI genes:
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