cocoon syndrome

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's subclass of is recorded as syndrome^[5].
• cocoon syndrome's subclass of is recorded as syndrome with limb malformations as a major feature^[6].
• cocoon syndrome's subclass of is recorded as rare genetic developmental defect during embryogenesis^[7].
• cocoon syndrome's subclass of is recorded as genetic disease^[8].
• cocoon syndrome's OMIM ID is recorded as 613630^[9].
• cocoon syndrome's KEGG ID is recorded as H00882^[10].
• cocoon syndrome's Disease Ontology ID is recorded as DOID:0060647^[11].
• cocoon syndrome's Orphanet ID is recorded as 465824^[12].
• cocoon syndrome's genetic association is recorded as CHUK^[13].
• cocoon syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060647^[14].
• cocoon syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060647^[15].
• cocoon syndrome's UMLS CUI is recorded as C3150891^[16].
• cocoon syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine^[17].
• cocoon syndrome's Mondo ID is recorded as MONDO_0013334^[18].
• cocoon syndrome's UniProt disease ID is recorded as DI-02978^[19].