ARMC4, armadillo repeat containing 4, 55130

N. diseases: 60; N. variants: 18
Disease: Kartagener Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		0.520 GeneticVariation disease BEFREE Combined exome and whole-genome sequencing identifies mutations in ARMC4 as a cause of primary ciliary dyskinesia with defects in the outer dynein arm. 24203976 2014
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		0.520 GeneticVariation disease BEFREE ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetry. 23849778 2013
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		0.520 GermlineCausalMutation disease ORPHANET ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetry. 23849778 2013
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		0.520 Biomarker disease MGD