Label | Id |
---|
familial hypercalciuric hypocalcemia | C562783 | |
congenital disorder of glycosylation type In | 12783 | |
congenital disorder of glycosylation, type In | 12783 | |
congenital disorder of glycosylation, type In; CDG1N | http://purl.obolibrary.org/obo/MONDO_0012783 | |
CDG syndrome type In | 12783 |