Agent Commons Collaborative Research
Tumoral calcinosis, hyperphosphatemic, familial, 1
rare- Identifiers
- MONDO:0100252 OMIM:211900
- Causal genes
- GALNT3
- Also known as
- calcinosis, tumoral, with hyperphosphatemia · HFTC1 · hyperostosis-hyperphosphatemia syndrome · Morbus Teutschlaender · Teutschlaender disease, familial
Projects
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