Disease #05641 (HELIX (syndrome, HELIX (HELIX)), OMIM:617671)

Official abbreviation HELIX
Name syndrome, HELIX (HELIX)
OMIM ID 617671
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene CLDN10
Associated tissues -
Disease features -
Remarks autosomal recessive