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KHDC3L

KH domain containing 3 like, subcortical maternal complex member

HCNC Approved Symbol
KHDC3L (HGNC:33699)
Genomic Coordinates
6:73,362,658 - 73,364,171 (6q13)
Synonyms
ECAT1, C6orf221
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Hydatidiform mole, recurrent, 2
614293AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the KHDC3L gene.

Frequently observed phenotypes

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

No Results