Disease #04397 (HRPT1 (hyperparathyroidism, familial primary, type 1 (HRPT-1)), OMIM:145000)

Official abbreviation HRPT1
Name hyperparathyroidism, familial primary, type 1 (HRPT-1)
OMIM ID 145000
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 11
Phenotype entries for this disease 10
Associated with 1 gene CDC73
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

11 entries on 1 page. Showing entries 1 - 11.
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00204819 - - - - ? - - - - - - HRPT1 - CASR CASR 1 1 LOVD
00204857 - - - - ? - - - - - - HRPT1 - CASR CASR 1 1 LOVD
00204896 - - - - ? - - - - - - HRPT1 - CASR CASR 1 1 LOVD
00204925 - - - - ? - - - - - - HRPT1 - CASR CASR 1 1 LOVD
00204927 - - - - ? - - - - - - HRPT1 - CASR CASR 1 1 LOVD
00204929 - - - - ? - - - - - - HRPT1 - CASR CASR 1 1 LOVD
00204932 - - - - ? - - - - - - HRPT1 - CASR CASR 1 1 LOVD
00204941 - - - - ? - - - - - - HRPT1 - CASR CASR 1 1 LOVD
00205007 - - - - ? - - - - - - HRPT1 - CASR CASR 1 1 LOVD
00205025 - - - - ? - - - - - - HRPT1 - CASR CASR 1 1 LOVD
00205098 - - - - ? - - - - - - HRPT1 - CASR CASR 1 1 LOVD
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