Hearing loss, autosomal recessive

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Subtype of: Hearing loss
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
hearing loss, autosomal recessive
MONDO:0019588MONDO_0019588
PDZD7 Causal — ClinGen —
PTPRQ Causal — ClinGen —
TRIOBP Causal — ClinGen —
DMXL2 Unknown
25248098 31688942 30237576 22875945 27657680
Open Targets
PPIP5K2 Unknown — ClinGen
SLC22A4 Unknown — ClinGen
TMEM132E Unknown — ClinGen —
WBP2 Unknown — ClinGen —
All8 Causal3 Unknown5
Related Diseases Diseases that share the most curated genes with Hearing loss, autosomal recessive.
5 View disease cluster →
Ohtahara syndrome 1 shared geneDMXL2 Related via 1 shared gene including DMXL2. Epileptic encephalopathy, early infantile, 81 1 shared geneDMXL2 Related via 1 shared gene including DMXL2. Polyendocrine-polyneuropathy syndrome 1 shared geneDMXL2 Related via 1 shared gene including DMXL2. Deafness, autosomal recessive 28 1 shared geneTRIOBP Related via 1 shared gene including TRIOBP. Deafness, autosomal dominant 73 1 shared genePTPRQ Related via 1 shared gene including PTPRQ.