autosomal dominant hypocalcemia 2 (Q30989619)
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autosomal dominant hypocalcemia disease that has material basis in heterozygous mutation in the GNA11 gene on chromosome 19p13
- HYPOC2
- HYPOCALCEMIA, AUTOSOMAL DOMINANT 2
- HYPOCALCEMIA, AUTOSOMAL DOMINANT 2; HYPOC2
- Hypocalcemia, Autosomal Dominant type 2
- autosomal dominant hypocalcemia type 2
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal dominant hypocalcemia 2 |
autosomal dominant hypocalcemia disease that has material basis in heterozygous mutation in the GNA11 gene on chromosome 19p13 |
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Statements
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Identifiers
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1 reference