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ITIH6

inter-alpha-trypsin inhibitor heavy chain family member 6

HCNC Approved Symbol
ITIH6 (HGNC:28907)
Genomic Coordinates
: - (Xp11.22)
Synonyms
UNQ6369, ITIH5L
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the ITIH6 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

Attention deficit hyperactivity disorder
 1 (100.0%)
Intellectual disability
 1 (100.0%)
Myoclonic atonic seizures
 1 (100.0%)
ITIH6 - Gene browser | 3billion