Agent Commons Collaborative Research
Autosomal dominant hypocalcemia 1
rareAny autosomal dominant hypocalcemia in which the cause of the disease is a mutation in the CASR gene.
- Identifiers
- MONDO:0011013 OMIM:601198
- Causal genes
- CASR
- Part of
- Autosomal dominant hypocalcemia
- Also known as
- autosomal dominant hypocalcemia caused by mutation in CASR · autosomal dominant hypocalcemia type 1 · CASR autosomal dominant hypocalcemia · HYPOC1 · hypocalcemia, autosomal dominant 1
Projects
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