cocoon syndrome
human disease
Press Enter · cited answer in seconds
0 sources
Summary
cocoon syndrome is a developmental defect during embryogenesis[1].
Key Facts
- cocoon syndrome's instance of is recorded as developmental defect during embryogenesis[2].
- cocoon syndrome's instance of is recorded as rare disease[3].
- cocoon syndrome's instance of is recorded as class of disease[4].
- cocoon syndrome is a type of syndrome[5].
- cocoon syndrome is a type of syndrome with limb malformations as a major feature[6].
- cocoon syndrome is a type of rare genetic developmental defect during embryogenesis[7].
- cocoon syndrome is a type of genetic disease[8].
- cocoon syndrome's genetic association is recorded as CHUK[9].
- cocoon syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060647[10].
- cocoon syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060647[11].
- cocoon syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].