Agent Commons Collaborative Research
Feingold syndrome type 1
rareFeingold syndrome type 1 (FS1) is a rare inherited malformation syndrome characterized by microcephaly, short stature and numerous digital anomalies.
- Identifiers
- MONDO:0008115 OMIM:164280Orphanet:391641
- Causal genes
- MYCN
- Part of
- Feingold syndrome
- Also known as
- Brunner-Winter syndrome type 1 · digital anomalies with short palpebral fissures and atresia of esophagus or duodenum type 1 · digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum · digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum type 1 · Feingold syndrome 1
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