Term info
database cross reference
- Orphanet:471383 (MONDO:equivalentTo)
Subsets
disease_grouping, ordo_group_of_disorders
definition
An instance of lethal multiple congenital anomalies/dysmorphic syndrome that is caused by an inherited modification of the individual's genome.
exactMatch
http://purl.obolibrary.org/obo/Orphanet_471383
has exact synonym
hereditary lethal multiple congenital anomalies/dysmorphic syndrome
id
MONDO:0043009