developmental defect during embryogenesis
Go to external page http://purl.obolibrary.org/obo/MONDO_0019755
A disease that has its basis in the disruption of embryonic morphogenesis. [ MONDO:design_pattern ]
Synonyms: embryonic morphogenesis disease rare developmental defect during embryogenesis malformation syndrome congenital malformation syndrome developmental defect during embryogenesis disorder of embryonic morphogenesis
Term information
- SCTID:400038003 (MONDO:equivalentTo)
- ICD9:759.7
- GARD:22513 (Orphanet:93890)
- NCIT:C99267 (MONDO:equivalentTo)
- Orphanet:93890 (MONDO:equivalentTo)
gard_rare, disease_grouping, rare, orphanet_rare, ordo_group_of_disorders
http://purl.obolibrary.org/obo/NCIT_C99267
http://www.orpha.net/ORDO/Orphanet_93890
http://identifiers.org/snomedct/400038003