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: C1281440
Disease: Familial obesity
Familial obesity
0 3 0 0 1 9.1E-02
CUI: C2937224
Disease: Constitutional obesity
Constitutional obesity
0 3 0 0 1 9.1E-02
CUI: C3825462
Disease: Diabetes in youth
Diabetes in youth
0 2 0 0 1 1.0E-01
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
850 0 1 1.1E-03 0 0
Sensorineural Hearing Loss (disorder)
783 0 1 1.2E-03 0 0
CUI: C1384666
Disease: hearing impairment
hearing impairment
740 0 1 1.3E-03 0 0
Finding of Mean Corpuscular Hemoglobin
653 0 1 1.5E-03 0 0
CUI: C0008925
Disease: Cleft Palate
Cleft Palate
611 0 1 1.5E-03 0 0
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia
559 0 1 1.7E-03 0 0
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
546 0 1 1.7E-03 0 0
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability
2165 0 4 1.8E-03 0 0
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma
507 0 1 1.8E-03 0 0
CUI: C0025362
Disease: Mental Retardation
Mental Retardation
505 0 1 1.9E-03 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria
487 0 1 1.9E-03 0 0
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus
473 0 1 2.0E-03 0 0
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
473 0 1 2.0E-03 0 0
CUI: C0032927
Disease: Precancerous Conditions
Precancerous Conditions
471 0 1 2.0E-03 0 0
CUI: C0349566
Disease: Squamous cell carcinoma of tongue
Squamous cell carcinoma of tongue
462 0 1 2.0E-03 0 0
CUI: C0235946
Disease: Cerebral atrophy
Cerebral atrophy
454 0 1 2.0E-03 0 0
CUI: C0013421
Disease: Dystonia
Dystonia
453 0 1 2.0E-03 0 0
CUI: C0557874
Disease: Global developmental delay
Global developmental delay
1825 0 4 2.2E-03 0 0
CUI: C0022104
Disease: Irritable Bowel Syndrome
Irritable Bowel Syndrome
429 0 1 2.2E-03 0 0
CUI: C0343641
Disease: Human papilloma virus infection
Human papilloma virus infection
429 0 1 2.2E-03 0 0
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects
426 0 1 2.2E-03 0 0
CUI: C0009806
Disease: Constipation
Constipation
424 0 1 2.2E-03 0 0