Hearing loss, autosomal recessive

Log in to bookmark this disease

Bookmark This Disease

Subtype of: Hearing loss
Show the subtypes
Download as CSV Download as PDF
Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
hearing loss, autosomal recessive
MONDO_0019588MONDO:0019588
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.