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DHX37

DEAH-box helicase 37

HCNC Approved Symbol
DHX37 (HGNC:17210)
Genomic Coordinates
12:124,946,826 - 124,989,131 (12q24.31)
Synonyms
KIAA1517, MGC4322, MGC2695, Dhr1, DDX37
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
46XY sex reversal 11
273250AD
Neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies
618731AR

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the DHX37 gene.

Frequently observed phenotypes

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

Ambiguous genitalia
 2 (100.0%)
Abnormal sex determination
 1 (50.0%)
Absent uterus
 1 (50.0%)
Absent/underdeveloped fallopian tube
 1 (50.0%)
Congenital cataract
 1 (50.0%)