CDC14A, cell division cycle 14A, 8556

N. diseases: 26; N. variants: 8
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 32 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1837608
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 32
DEAFNESS, AUTOSOMAL RECESSIVE 32 		0.700 GeneticVariation disease UNIPROT CDC14A phosphatase is essential for hearing and male fertility in mouse and human. 29293958 2018
CUI: C1837608
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 32
DEAFNESS, AUTOSOMAL RECESSIVE 32 		0.700 CausalMutation disease CLINVAR CDC14A phosphatase is essential for hearing and male fertility in mouse and human. 29293958 2018
CUI: C1837608
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 32
DEAFNESS, AUTOSOMAL RECESSIVE 32 		0.700 Biomarker disease CTD_human CDC14A phosphatase is essential for hearing and male fertility in mouse and human. 29293958 2018
CUI: C1837608
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 32
DEAFNESS, AUTOSOMAL RECESSIVE 32 		0.700 GeneticVariation disease CLINVAR CDC14A phosphatase is essential for hearing and male fertility in mouse and human. 29293958 2018
CUI: C1837608
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 32
DEAFNESS, AUTOSOMAL RECESSIVE 32 		0.700 Biomarker disease GENOMICS_ENGLAND Mutations in CDC14A, Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound Deafness. 27259055 2016
CUI: C1837608
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 32
DEAFNESS, AUTOSOMAL RECESSIVE 32 		0.700 Biomarker disease CTD_human Mutations in CDC14A, Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound Deafness. 27259055 2016
CUI: C1837608
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 32
DEAFNESS, AUTOSOMAL RECESSIVE 32 		0.700 CausalMutation disease CLINVAR Mutations in CDC14A, Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound Deafness. 27259055 2016
CUI: C1837608
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 32
DEAFNESS, AUTOSOMAL RECESSIVE 32 		0.700 GeneticVariation disease UNIPROT Mutations in CDC14A, Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound Deafness. 27259055 2016