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hypercholanemia, familial, 2 | RareConnect | RareConnect.io

/hypercholanemia, familial

/hypercholanemia, familial, 2

hypercholanemia, familial, 2

Rare Disease

MONDO:0031003

Also Known As

FHCA2NTCP Deficiencyhypercholanemia, familial 2

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

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

External Resources

OMIM

OMIM:619256 ↗

GARD

Related Diseases

hypercholanemia, familial 1

MONDO:0031446

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