CDC14A

Name: CDC14A
HGNC ID: HGNC:1718
Cytogenetic Location: 1p21.2

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ClinVar Variants: View ClinVar Variants
GeneReviews®: View GeneReviews

CDC14A - hearing impairment and infertile male syndrome | MONDO:0100069

Curated by	Classification		Date	Report
Gene-Disease Validity	Strong	Autosomal Recessive	03/11/2020	View report

CDC14A - nonsyndromic genetic deafness | MONDO:0019497

Curated by	Classification		Date	Report
Gene-Disease Validity	Limited	Autosomal Recessive	02/26/2018	View report