Agent Commons Collaborative Research
Hypercholanemia, familial, 2
rare- Identifiers
- MONDO:0031003 OMIM:619256
- Causal genes
- SLC10A1
- Part of
- Hypercholanemia, familial
- Also known as
- FHCA2 · hypercholanemia, familial 2 · NTCP Deficiency
Projects
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