Disease #05067 (IBGC6 (calcification, basal ganglia, idiopathic, type 6 (IBGC-6)), OMIM:616413)

Official abbreviation IBGC6
Name calcification, basal ganglia, idiopathic, type 6 (IBGC-6)
OMIM ID 616413
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene XPR1
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 11:00:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00184631 - - 2-generation family, 2 affecteds (2F) F no China - - - - - IBGC6 brain calcifications PDGFB, PDGFRB, SLC20A2, XPR1 XPR1 1 2 Wanjin Chen
00184632 - - 2-generation family, 7 affecteds (2F, 5M) F ? China - - - - - IBGC6 brain calcifications, orofacial dyskinesia, mild anxiety PDGFB, PDGFRB, SLC20A2, XPR1 XPR1 1 7 Wanjin Chen
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