Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B
12 0 1 8.3E-02 0 0
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder)
12 0 1 8.3E-02 0 0
Night blindness, congenital stationary, type 1
12 0 1 8.3E-02 0 0
Night Blindness, Congenital Stationary, Type 1A
13 0 1 7.7E-02 0 0
CUI: C3711543
Disease: X-Linked Csnb
X-Linked Csnb
13 0 1 7.7E-02 0 0
Cone-rod synaptic disorder, congenital nonprogressive
14 0 1 7.1E-02 0 0
CUI: C4024756
Disease: Abnormality of macular pigmentation
Abnormality of macular pigmentation
25 0 1 4.0E-02 0 0
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A
26 0 1 3.8E-02 0 0
CUI: C1298695
Disease: Hypoplasia of optic disc
Hypoplasia of optic disc
31 0 1 3.2E-02 0 0
Night blindness, congenital stationary
32 0 1 3.1E-02 0 0
CUI: C2678065
Disease: Myofibrillar Myopathy
Myofibrillar Myopathy
61 0 1 1.6E-02 0 0
CUI: C2937358
Disease: Cerebral Hemorrhage
Cerebral Hemorrhage
122 0 1 8.2E-03 0 0
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity
147 0 1 6.8E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia
168 0 1 6.0E-03 0 0
CUI: C0271183
Disease: Severe myopia
Severe myopia
184 0 1 5.4E-03 0 0
CUI: C0456909
Disease: Blindness
Blindness
393 0 1 2.5E-03 0 0
CUI: C0015397
Disease: Disorder of eye
Disorder of eye
400 0 1 2.5E-03 0 0
Corpuscular Hemoglobin Concentration Mean
401 0 1 2.5E-03 0 0
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
546 541 1 1.8E-03 1 1.8E-03
Finding of Mean Corpuscular Hemoglobin
653 0 1 1.5E-03 0 0
CUI: C0035309
Disease: Retinal Diseases
Retinal Diseases
714 0 1 1.4E-03 0 0
CUI: C0038379
Disease: Strabismus
Strabismus
716 0 1 1.4E-03 0 0
CUI: C1963184
Disease: Nystagmus, CTCAE 3.0
Nystagmus, CTCAE 3.0
779 0 1 1.3E-03 0 0
CUI: C4554036
Disease: Nystagmus, CTCAE 5.0
Nystagmus, CTCAE 5.0
779 0 1 1.3E-03 0 0
CUI: C0028738
Disease: Nystagmus
Nystagmus
833 0 1 1.2E-03 0 0