OTOGL, otogelin like, 283310

N. diseases: 9; N. variants: 8
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 84B ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3554159
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 84B
DEAFNESS, AUTOSOMAL RECESSIVE 84B 		0.600 Biomarker disease GENOMICS_ENGLAND Mutations in OTOGL, encoding the inner ear protein otogelin-like, cause moderate sensorineural hearing loss. 23122586 2012
CUI: C3554159
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 84B
DEAFNESS, AUTOSOMAL RECESSIVE 84B 		0.600 Biomarker disease CTD_human
CUI: C3554159
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 84B
DEAFNESS, AUTOSOMAL RECESSIVE 84B 		0.600 Biomarker disease GENOMICS_ENGLAND
CUI: C3554159
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 84B
DEAFNESS, AUTOSOMAL RECESSIVE 84B 		0.600 CausalMutation disease CLINVAR
CUI: C3554159
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 84B
DEAFNESS, AUTOSOMAL RECESSIVE 84B 		0.600 GeneticVariation disease CLINVAR