hearing loss, autosomal recessive

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
hearing loss, autosomal recessive
PDZD7 Causal — ClinGen —
PTPRQ Causal — ClinGen —
TRIOBP Causal — ClinGen —
PPIP5K2 Unknown — ClinGen
SLC22A4 Unknown — ClinGen
TMEM132E Unknown — ClinGen —
WBP2 Unknown — ClinGen —
All7 Causal3 Unknown4
Related Diseases Diseases that share the most curated genes with hearing loss, autosomal recessive.
5 View disease cluster →
Pericardium disorder 1 shared genePTPRQ Related via 1 shared gene including PTPRQ. Congenital hearing disorder 1 shared geneSLC22A4 Related via 1 shared gene including SLC22A4. Congenital ear anomaly 2 shared genesPTPRQ, PDZD7 Related via 2 shared genes including PTPRQ, PDZD7. Congenital pes cavus 1 shared genePTPRQ Related via 1 shared gene including PTPRQ. Isolated sensorineural deafness 5 shared genesTRIOBP, PTPRQ, PPIP5K2, TMEM132E, WBP2 Related via 5 shared genes including TRIOBP, PTPRQ, PPIP5K2.