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: C0234244
Disease: Tissue Pain
Tissue Pain
1 0 1 3.2E-03 0 0
CUI: C0234505
Disease: Tactile Agnosia
Tactile Agnosia
1 0 1 3.2E-03 0 0
CUI: C0235146
Disease: Euphoric mood
Euphoric mood
1 0 1 3.2E-03 0 0
CUI: C0235832
Disease: Congenital hernia
Congenital hernia
1 0 1 3.2E-03 0 0
CUI: C0235910
Disease: Colagenosis
Colagenosis
1 0 1 3.2E-03 0 0
Disorder of male reproductive system
1 0 1 3.2E-03 0 0
CUI: C0239846
Disease: Hand-wringing
Hand-wringing
1 0 1 3.2E-03 0 0
CUI: C0241950
Disease: Intestinal infarction
Intestinal infarction
1 0 1 3.2E-03 0 0
CUI: C0242036
Disease: Paraplegia, Ataxic
Paraplegia, Ataxic
1 0 1 3.2E-03 0 0
CUI: C0262477
Disease: Eye problem
Eye problem
1 0 1 3.2E-03 0 0
CUI: C0263442
Disease: Acne Conglobata
Acne Conglobata
1 0 1 3.2E-03 0 0
Osteoarthropathy of fingers familial
1 0 1 3.2E-03 0 0
CUI: C0264954
Disease: Arteriovascular degeneration
Arteriovascular degeneration
1 0 1 3.2E-03 0 0
Spondylometaphyseal dysplasia, Kozlowski type
1 0 1 3.2E-03 0 0
CUI: C0265281
Disease: Metatropic dwarfism
Metatropic dwarfism
1 0 1 3.2E-03 0 0
CUI: C0265404
Disease: 4q partial monosomy syndrome
4q partial monosomy syndrome
1 0 1 3.2E-03 0 0
CUI: C0266384
Disease: Congenital absence of uterus
Congenital absence of uterus
1 0 1 3.2E-03 0 0
CUI: C0266429
Disease: Monorchism
Monorchism
1 0 1 3.2E-03 0 0
CUI: C0266430
Disease: Polyorchism
Polyorchism
1 0 1 3.2E-03 0 0
CUI: C0266692
Disease: Craniopagus
Craniopagus
1 0 1 3.2E-03 0 0
Classical galactosemia, homozygous Duarte-type
1 0 1 3.2E-03 0 0
CUI: C0268357
Disease: Osteogenesis imperfecta, type 1A
Osteogenesis imperfecta, type 1A
1 0 1 3.2E-03 0 0
CUI: C0270149
Disease: Perinatal respiratory distress
Perinatal respiratory distress
1 0 1 3.2E-03 0 0
CUI: C0270150
Disease: Perinatal respiratory failure
Perinatal respiratory failure
1 0 1 3.2E-03 0 0
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis
1 0 1 3.2E-03 0 0