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Online Mendelian Inheritance in Man
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/OMIM/164280
http://purl.bioontology.org/ontology/OMIM/164280
|
|---|---|
| Preferred Name | FEINGOLD SYNDROME 1 |
| Synonyms |
MICROCEPHALY, MENTAL RETARDATION, AND TRACHEOESOPHAGEAL FISTULA SYNDROME
MICROCEPHALY-OCULO-DIGITO-ESOPHAGEAL-DUODENAL SYNDROME
DIGITAL ANOMALIES WITH SHORT PALPEBRAL FISSURES AND ATRESIA OF ESOPHAGUS OR DUODENUM
MODED
OCULODIGITOESOPHAGODUODENAL SYNDROME
FGLDS1
MMT SYNDROME
FEINGOLD SYNDROME
ODED SYNDROME
MICROCEPHALY AND DIGITAL ABNORMALITIES WITH NORMAL INTELLIGENCE
ODED
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|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel | MICROCEPHALY, MENTAL RETARDATION, AND TRACHEOESOPHAGEAL FISTULA SYNDROME
MICROCEPHALY-OCULO-DIGITO-ESOPHAGEAL-DUODENAL SYNDROME
DIGITAL ANOMALIES WITH SHORT PALPEBRAL FISSURES AND ATRESIA OF ESOPHAGUS OR DUODENUM
MODED
OCULODIGITOESOPHAGODUODENAL SYNDROME
FGLDS1
MMT SYNDROME
FEINGOLD SYNDROME
ODED SYNDROME
MICROCEPHALY AND DIGITAL ABNORMALITIES WITH NORMAL INTELLIGENCE
ODED
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|
|---|---|
| prefLabel | FEINGOLD SYNDROME 1
|
| Gene Symbol |
NMYC
MYCN
MPAPA
FGLDS1
|
| Scope Statement | Caused by mutations in the neuroblastoma-derived V-myc avian myelocytomatosis viral-related oncogene (MYCN, 164840.0001) [MOLECULAR BASIS]
|
| type | |
| Has manifestation |
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|
| tui | T047
|
| Gene Locus | 2p24.1
|
| MIMTYPEMEANING | Phenotype description, molecular basis known.
|
| notation | 164280
|
| Semantic type UMLS property | |
| Has inheritance type | |
| cui |
C4551774
C0796068
|
| Moved from | 602585
|
| OMIM Entry Type | 3
|
| OMIM MimType Value | pound
|
| Delete | Subject | Author | Type | Created |
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| No notes to display |