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Summary Literature (0)
MIM:608653 - DEAFNESS, AUTOSOMAL RECESSIVE 32, WITH OR WITHOUT IMMOTILE SPERM; DFNB32

Xenbase Genes: cdc14a

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012091 - autosomal recessive nonsyndromic hearing loss 32
MONDO:0019588 - hearing loss, autosomal recessive

Disease Ontology (DO):
DOID:0110491 - autosomal recessive nonsyndromic deafness 32