loading...| Preferred Name |
genetic multiple congenital anomalies/dysmorphic syndrome |
|
| Synonyms |
hereditary multiple congenital anomalies/dysmorphic syndrome |
|
| Definitions |
An instance of multiple congenital anomalies/dysmorphic syndrome that is caused by an inherited modification of the individual's genome. |
|
| ID |
http://purl.obolibrary.org/obo/MONDO_0043005 |
|
| conformsTo |
http://purl.obolibrary.org/obo/mondo/patterns/hereditary.yaml |
|
| database_cross_reference |
Orphanet:183533 |
|
| exactMatch | ||
| has exact synonym |
hereditary multiple congenital anomalies/dysmorphic syndrome |
|
| has modifier | ||
| id |
MONDO:0043005 |
|
| imported from | ||
| in_subset |
http://purl.oboInOwllibrary.org/oboInOwl/mondo#ordo_group_of_disorders |
|
| label |
genetic multiple congenital anomalies/dysmorphic syndrome |
|
| notation |
MONDO:0043005 |
|
| prefLabel |
genetic multiple congenital anomalies/dysmorphic syndrome |
|
| textual definition |
An instance of multiple congenital anomalies/dysmorphic syndrome that is caused by an inherited modification of the individual's genome. |
|
| subClassOf |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.obolibrary.org/obo/MONDO_0043005 | MONDO | SAME_URI | |
| http://purl.obolibrary.org/obo/MONDO_0043005 | EFO | SAME_URI | |
| http://www.limics.org/hrdo/rdfns#pat_id_18264 | HRDO | LOOM | |
| http://www.orpha.net/ORDO/Orphanet_183533 | ORDO | LOOM |