Neonatal ichthyosis–sclerosing cholangitis syndrome
Neonatal ichthyosis–sclerosing cholangitis syndrome | |
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Classification and external resources | |
OMIM | 607626 |
Neonatal ichthyosis–sclerosing cholangitis syndrome (also known as "NISCH syndrome"[1] and "ichthyosis–sclerosing cholangitis syndrome"[1]) is a cutaneous condition caused by mutations in the Claudin 1 gene.[1]
See also
References
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