Cell Culture Ontology

Last uploaded: July 23, 2014

Preferred Name
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
database_cross_reference	GARD:19444 MESH:D000083083 UMLS:C5392094 Orphanet:98301
definition	A rare genetic disorder caused by mutations in genes encoding proteins of the nuclear lamina.
exactMatch	http://purl.obolibrary.org/obo/Orphanet_98301 http://linkedlifedata.com/resource/umls/id/C5392094 http://identifiers.org/mesh/D000083083
id	MONDO:0021106
in_subset	http://purl.obolibrary.org/obo/mondo#rare http://purl.obolibrary.org/obo/mondo#orphanet_rare http://purl.obolibrary.org/obo/mondo#gard_rare http://purl.obolibrary.org/obo/mondo#disease_grouping http://purl.obolibrary.org/obo/mondo#ordo_group_of_disorders
label	laminopathy
notation	MONDO:0021106
subClassOf	http://www.ebi.ac.uk/efo/EFO_0000508

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