Preferred Label : Basal ganglia calcification, idiopathic, 2;
Obsolete resource : true;
Moved to : 213600;
Symbol : IBGC2;
CISMeF acronym : IBGC2;
Type : Phenotype or locus, molecular basis unknown;
Description : Familial idiopathic basal ganglia calcification (IBGC) is characterized by bilateral
basal ganglia calcification and has been associated with a variety of neurologic,
cognitive, and psychiatric abnormalities. However, some affected individuals may be
clinically asymptomatic (summary by Volpato et al., 2009). For a detailed phenotypic
description and a discussion of genetic heterogeneity of IBGC, see IBGC1 (213600).;
Prefixed ID : 606656;
Origin ID : 606656;
UMLS CUI : C1847731;
Currated CISMeF NLP mapping
Semantic type(s)
UMLS correspondences (same concept)