| Metadata | |
|---|---|
| ID | DOID:0060464 |
| Name | Feingold syndrome |
| Definition | A syndrome characterized by variable combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and learning disability/mental retardation. http://ghr.nlm.nih.gov/condition/feingold-syndrome, https://www.ncbi.nlm.nih.gov/pubmed/16906565, https://www.ncbi.nlm.nih.gov/pubmed/14518066, https://en.wikipedia.org/wiki/Feingold_syndrome |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Synonyms |
digital anomalies with short palpebral fissures and atresia of esophagus or duodenum [EXACT] FGLDS [EXACT] microcephaly-digital anomalies-normal intelligence syndrome [EXACT] microcephaly-oculo-digito-esophageal-duodenal syndrome [EXACT] MODED syndrome [EXACT] oculo-digito-esophageal-duodenal syndrome [EXACT] ODED syndrome [EXACT] |
| Parent Relationships |
is_a autosomal dominant disease is_a syndrome |
| Subclass Logical Relationships |
has material basis in some autosomal dominant inheritance |