An instance of hyperparathyroidism that is caused by an inherited genomic modification in an individual. [ MONDO:patterns/hereditary ]

Synonyms: genetic hyperparathyroidism

This is just here as a test because I lose it

Term information

database cross reference
  • Orphanet:208596 (MONDO:equivalentTo)
  • GARD:20408 (Orphanet:208596)
  • OMIMPS:145000 (MONDO:equivalentTo)
Subsets

gard_rare, disease_grouping, rare, orphanet_rare, ordo_group_of_disorders

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/5114

exactMatch

https://omim.org/phenotypicSeries/PS145000

http://www.orpha.net/ORDO/Orphanet_208596

id

MONDO:0016166

Term relations