/autosomal dominant hypocalcemia 2

autosomal dominant hypocalcemia 2

Rare Disease

MONDO:0014146

Also Known As

HYPOC2autosomal dominant hypocalcemia type 2hypocalcemia, autosomal dominant type 2hypocalcemia, autosomal dominant 2

An autosomal dominant hypocalcemia disease that has material basis in heterozygous mutation in the GNA11 gene on chromosome 19p13.

Comprehensive, easy-to-understand information about this condition

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Gene data from MyGene.info • Click to view on NCBI Gene

autosomal dominant hypocalcemia 1

MONDO:0011013