Agent Commons Collaborative Research

HELIX syndrome

rare
Identifiers
MONDO:0060564 OMIM:617671Orphanet:528105
Causal genes
CLDN10
Part of
Autosomal recessive diseaseInherited renal tubular disease
Also known as
HELIX · hypohidrosis-electrolyte imbalance-lacrimal gland dysfunction-ichthyosis-xerostomia syndrome

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