Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C1866190
Disease: Atresia of the external auditory canal
Atresia of the external auditory canal 		44 0 1 1.0E-03 0 0
CUI: C0152191
Disease: Scotoma, Central
Scotoma, Central 		43 0 1 1.0E-03 0 0
CUI: C0429097
Disease: QRS complex feature
QRS complex feature 		41 0 1 1.0E-03 0 0
CUI: C0581354
Disease: Recurrent sinusitis
Recurrent sinusitis 		41 0 1 1.0E-03 0 0
CUI: C2677650
Disease: Decreased activity of mitochondrial complex I
Decreased activity of mitochondrial complex I 		41 0 1 1.0E-03 0 0
CUI: C3278975
Disease: Attenuation of retinal blood vessels
Attenuation of retinal blood vessels 		41 0 1 1.0E-03 0 0
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		40 0 1 1.0E-03 0 0
CUI: C0432163
Disease: Defect of vertebral segmentation
Defect of vertebral segmentation 		40 0 1 1.0E-03 0 0
CUI: C1956147
Disease: Microlissencephaly
Microlissencephaly 		40 0 1 1.0E-03 0 0
CUI: C4021608
Disease: Shortening of all distal phalanges of the fingers
Shortening of all distal phalanges of the fingers 		40 0 1 1.0E-03 0 0
CUI: C0431350
Disease: Primary microcephaly
Primary microcephaly 		39 0 1 1.0E-03 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		39 0 1 1.0E-03 0 0
CUI: C4021546
Disease: Abnormal mitochondria in muscle tissue
Abnormal mitochondria in muscle tissue 		39 0 1 1.0E-03 0 0
CUI: C0266011
Disease: Accessory nipple
Accessory nipple 		38 0 1 1.0E-03 0 0
CUI: C0003028
Disease: Anhidrosis
Anhidrosis 		37 0 1 1.0E-03 0 0
CUI: C0431362
Disease: Lobar Holoprosencephaly
Lobar Holoprosencephaly 		37 0 1 1.0E-03 0 0
CUI: C0018810
Disease: heart rate
heart rate 		36 0 1 1.0E-03 0 0
CUI: C0266667
Disease: Cyclocephaly
Cyclocephaly 		35 0 1 1.0E-03 0 0
CUI: C1833144
Disease: Slender long bone
Slender long bone 		35 0 1 1.0E-03 0 0
CUI: C1846151
Disease: Widened subarachnoid space
Widened subarachnoid space 		35 0 1 1.0E-03 0 0
CUI: C3853041
Disease: Severe Congenital Microcephaly
Severe Congenital Microcephaly 		35 0 1 1.0E-03 0 0
CUI: C4543926
Disease: Narcolepsy type 1
Narcolepsy type 1 		35 0 1 1.0E-03 0 0
CUI: C0685891
Disease: Congenital hypoplasia of thymus
Congenital hypoplasia of thymus 		34 0 1 1.0E-03 0 0
CUI: C1838705
Disease: Anteriorly placed anus
Anteriorly placed anus 		34 0 1 1.0E-03 0 0
CUI: C2675021
Disease: Narrow palpebral fissure
Narrow palpebral fissure 		34 0 1 1.0E-03 0 0