Autosomal recessive nonsyndromic hearing loss 63

Log in to bookmark this disease

Bookmark This Disease

Subtype of: Hearing loss, autosomal recessive · Nonsyndromic hearing loss
Download as CSV Download as PDF
Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
autosomal recessive nonsyndromic hearing loss 63
MONDO:0012670
LRTOMT Causal — ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Autosomal recessive nonsyndromic hearing loss 63.
5 View disease cluster →
Deafness, autosomal recessive, 63 1 shared geneLRTOMT Related via 1 shared gene including LRTOMT. Hereditary hearing loss 1 shared geneLRTOMT Related via 1 shared gene including LRTOMT. Isolated sensorineural deafness 1 shared geneLRTOMT Related via 1 shared gene including LRTOMT. Nonsyndromic hearing loss 1 shared geneLRTOMT Related via 1 shared gene including LRTOMT. Nonsyndromic intellectual disability 1 shared geneLRTOMT Related via 1 shared gene including LRTOMT.