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C18orf32

chromosome 18 open reading frame 32

HCNC Approved Symbol
C18orf32 (HGNC:31690)
Genomic Coordinates
18:49,477,243 - 49,487,234 (18q21.1)
Synonyms
FLJ23458
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Glycosylphosphatidylinositol biosynthesis defect 25
619985AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the C18orf32 gene.

Frequently observed phenotypes

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

No Results