rs201943194, DNAH11

N. diseases: 38
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Atelectasis
CUI: C0004144
Disease: Atelectasis
0.700 CausalMutation CLINVAR
Spontaneous pneumothorax
CUI: C0149781
Disease: Spontaneous pneumothorax
0.700 CausalMutation CLINVAR
Abnormal ciliary motility
CUI: C4022983
Disease: Abnormal ciliary motility
0.700 CausalMutation CLINVAR
Acute bronchitis
CUI: C0149514
Disease: Acute bronchitis
0.700 CausalMutation CLINVAR
Chest Pain
CUI: C0008031
Disease: Chest Pain
0.700 CausalMutation CLINVAR
Recurrent otitis media
CUI: C0747085
Disease: Recurrent otitis media
0.700 CausalMutation CLINVAR
Rhinitis
CUI: C0035455
Disease: Rhinitis
0.700 CausalMutation CLINVAR
Melanocortin 4 Receptor Deficiency
CUI: C4054546
Disease: Melanocortin 4 Receptor Deficiency
0.700 CausalMutation CLINVAR
Dyspnea
CUI: C0013404
Disease: Dyspnea
0.700 CausalMutation CLINVAR
Asthma, Exercise-Induced
CUI: C0004099
Disease: Asthma, Exercise-Induced
0.700 CausalMutation CLINVAR
Large head (disorder)
CUI: C2243051
Disease: Large head (disorder)
0.700 CausalMutation CLINVAR
Recurrent pneumonia
CUI: C0694550
Disease: Recurrent pneumonia
0.700 CausalMutation CLINVAR
Scoliosis, unspecified
CUI: C0036439
Disease: Scoliosis, unspecified
0.700 CausalMutation CLINVAR