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: C4025720
Disease: Pseudobulbar behavioral symptoms
Pseudobulbar behavioral symptoms
5 0 5 0.56 0 0
CUI: C1853396
Disease: Primary lateral sclerosis juvenile
Primary lateral sclerosis juvenile
2 0 2 0.22 0 0
Abnormal upper motor neuron morphology
20 0 5 0.21 0 0
CUI: C0007528
Disease: Cecal Neoplasms
Cecal Neoplasms
5 0 2 0.17 0 0
CUI: C0153437
Disease: Malignant neoplasm of cecum
Malignant neoplasm of cecum
5 0 2 0.17 0 0
CUI: C2931117
Disease: Fetal megacystis
Fetal megacystis
5 4 2 0.17 2 0.50
Juvenile amyotrophic lateral sclerosis
20 0 4 0.16 0 0
CUI: C0232475
Disease: Decreased peristalsis
Decreased peristalsis
6 0 2 0.15 0 0
Abnormal lower motor neuron morphology
23 0 4 0.14 0 0
Functional abnormality of the gastrointestinal tract
7 0 2 0.14 0 0
CUI: C1853406
Disease: Difficulty in tongue movements
Difficulty in tongue movements
8 0 2 0.13 0 0
CUI: C1855311
Disease: Megacystis
Megacystis
8 0 2 0.13 0 0
AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE (disorder)
25 0 4 0.13 0 0
CUI: C0018809
Disease: Heart Neoplasm
Heart Neoplasm
17 0 3 0.13 0 0
CUI: C0042929
Disease: Polyp of vocal cord
Polyp of vocal cord
9 0 2 0.12 0 0
CUI: C0334448
Disease: Cellular Blue Nevus
Cellular Blue Nevus
9 0 2 0.12 0 0
CUI: C0393559
Disease: Troyer syndrome
Troyer syndrome
9 0 2 0.12 0 0
CUI: C1334260
Disease: Intramuscular Myxoma
Intramuscular Myxoma
9 0 2 0.12 0 0
Megacystis microcolon intestinal hypoperistalsis syndrome
9 0 2 0.12 0 0
CUI: C0154682
Disease: Lateral Sclerosis
Lateral Sclerosis
19 0 3 0.12 0 0
CUI: C0042781
Disease: Visceral Myopathy
Visceral Myopathy
10 19 2 0.12 2 0.11
CUI: C0030215
Disease: Palatal Neoplasms
Palatal Neoplasms
1 0 1 0.11 0 0
CUI: C0266200
Disease: Microcolon
Microcolon
11 2 2 0.11 2 1.00
CUI: C0271618
Disease: Delayed female puberty
Delayed female puberty
1 0 1 0.11 0 0
CUI: C0545081
Disease: mantle lymphoma
mantle lymphoma
1 0 1 0.11 0 0