An instance of hypoparathyroidism that is caused by an inherited genomic modification in an individual. [ MONDO:patterns/hereditary ]
Synonyms: genetic hypoparathyroidism
This is just here as a test because I lose it
Term information
database
cross reference
- UMLS:C5680825 (MONDO:equivalentTo)
- MEDGEN:1842344 (MONDO:equivalentTo)
- GARD:20407 (MONDO:GARD)
- Orphanet:208593 (MONDO:equivalentTo)
Subsets
gard_rare, otar, disease_grouping, rare, ordo_group_of_disorders
exactMatch
http://identifiers.org/medgen/1842344
http://www.orpha.net/ORDO/Orphanet_208593
http://linkedlifedata.com/resource/umls/id/C5680825