Preferred Name |
laminopathy |
|
Synonyms |
|
|
Definitions |
A rare genetic disorder caused by mutations in genes encoding proteins of the nuclear lamina. |
|
ID |
http://purl.obolibrary.org/obo/MONDO_0021106 |
|
definition |
A rare genetic disorder caused by mutations in genes encoding proteins of the nuclear lamina. |
|
label |
laminopathy |
|
prefixIRI |
MONDO:0021106 |
|
prefLabel |
laminopathy |
|
textual definition |
A rare genetic disorder caused by mutations in genes encoding proteins of the nuclear lamina. |
|
subClassOf |
Create mapping
Delete | Mapping To | Ontology | Source |
---|---|---|---|
http://purl.obolibrary.org/obo/MONDO_0021106 | MONDO | SAME_URI | |
http://purl.obolibrary.org/obo/MONDO_0021106 | EFO | SAME_URI | |
http://purl.obolibrary.org/obo/MONDO_0021106 | OBA | SAME_URI | |
http://purl.obolibrary.org/obo/MONDO_0021106 | MONDO | LOOM | |
http://www.limics.org/hrdo/rdfns#pat_id_13318 | HRDO | LOOM | |
http://www.orpha.net/ORDO/Orphanet_98301 | ORDO | LOOM | |
rgo:29958 | GAMUTS | LOOM | |
http://purl.obolibrary.org/obo/MONDO_0021106 | EFO | LOOM | |
http://purl.obolibrary.org/obo/MONDO_0021106 | OBA | LOOM | |
http://purl.jp/bio/4/id/200906070855184782 | IOBC | LOOM | |
http://www.orpha.net/ORDO/Orphanet_98301 | ORDO | LOOM |