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Summary Literature (0)
MIM:603629 - DEAFNESS, AUTOSOMAL RECESSIVE 21; DFNB21

Xenbase Genes: tecta.2, tecta

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011351 - autosomal recessive nonsyndromic hearing loss 21
MONDO:0019588 - hearing loss, autosomal recessive

Disease Ontology (DO):
DOID:0110479 - autosomal recessive nonsyndromic deafness 21