Terminology Service for NFDI4Health
genetic multiple congenital anomalies/dysmorphic syndrome
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http://purl.obolibrary.org/obo/MONDO_0043005
An instance of multiple congenital anomalies/dysmorphic syndrome that is caused by an inherited modification of the individual's genome. [ ]
Term info
Label
genetic multiple congenital anomalies/dysmorphic syndrome
Synonyms
- hereditary multiple congenital anomalies/dysmorphic syndrome
Subsets
disease_grouping, obsoletion_candidate, ordo_group_of_disorders
IAO 0006012
2022-09-01
comment
Reason: out of scope. MONDO:excludeGeneticFormOfDisease and MONDO:excludeGroupingClass. Term to consider: MONDO:0021147 disorder of development or morphogenesis
exactMatch
http://purl.obolibrary.org/obo/Orphanet_183533
id
MONDO:0043005
see also
https://github.com/monarch-initiative/mondo/issues/4069, https://github.com/monarch-initiative/mondo/issues/5114
Term relations
Subclass of: