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: C4021165
Disease: Abnormality of long bone morphology
Abnormality of long bone morphology 		3 0 3 0.38 0 0
CUI: C4023052
Disease: Ubiquitin-positive cerebral inclusion bodies
Ubiquitin-positive cerebral inclusion bodies 		3 0 3 0.38 0 0
CUI: C4025347
Disease: Weakness of muscles of respiration
Weakness of muscles of respiration 		4 0 3 0.33 0 0
CUI: C4024848
Disease: Absent pigmentation of the ventral chest
Absent pigmentation of the ventral chest 		2 0 2 0.25 0 0
CUI: C1863351
Disease: Calvarial hyperostosis
Calvarial hyperostosis 		10 0 3 0.20 0 0
CUI: C1836737
Disease: White eyebrow
White eyebrow 		7 0 2 0.15 0 0
CUI: C1836736
Disease: White eyelashes
White eyelashes 		8 0 2 0.14 0 0
CUI: C1839042
Disease: Upper motor neuron dysfunction
Upper motor neuron dysfunction 		16 0 3 0.14 0 0
CUI: C4021082
Disease: Fatty replacement of skeletal muscle
Fatty replacement of skeletal muscle 		17 0 3 0.14 0 0
CUI: C4025614
Disease: EMG: chronic denervation signs
EMG: chronic denervation signs 		18 0 3 0.13 0 0
CUI: C0178650
Disease: Gammopathy
Gammopathy 		1 0 1 0.12 0 0
CUI: C0206672
Disease: Hidrocystoma
Hidrocystoma 		1 0 1 0.12 0 0
CUI: C0263402
Disease: Telangiectasia macularis eruptiva perstans
Telangiectasia macularis eruptiva perstans 		1 0 1 0.12 0 0
CUI: C0334432
Disease: Nonpigmented nevus
Nonpigmented nevus 		1 0 1 0.12 0 0
CUI: C0341215
Disease: Gastroduodenal intussusception
Gastroduodenal intussusception 		1 0 1 0.12 0 0
CUI: C0343115
Disease: Skin Mastocytoma
Skin Mastocytoma 		1 0 1 0.12 0 0
CUI: C0375536
Disease: Congenital osteodystrophy
Congenital osteodystrophy 		1 0 1 0.12 0 0
CUI: C0413235
Disease: Idiopathic anaphylaxis
Idiopathic anaphylaxis 		1 0 1 0.12 0 0
CUI: C0521670
Disease: Cranial nerve compression
Cranial nerve compression 		19 0 3 0.12 0 0
CUI: C1275345
Disease: Familial mastocytosis
Familial mastocytosis 		1 0 1 0.12 0 0
CUI: C1333460
Disease: Esophageal Melanoma
Esophageal Melanoma 		1 0 1 0.12 0 0
CUI: C1333802
Disease: Gastrointestinal Stromal Tumor of the Gastrointestinal Tract
Gastrointestinal Stromal Tumor of the Gastrointestinal Tract 		1 0 1 0.12 0 0
CUI: C1334222
Disease: Intermediate Risk Gastrointestinal Stromal Tumor
Intermediate Risk Gastrointestinal Stromal Tumor 		1 0 1 0.12 0 0
CUI: C1336056
Disease: Spindle Cell Type Gastrointestinal Stromal Tumor
Spindle Cell Type Gastrointestinal Stromal Tumor 		1 0 1 0.12 0 0
CUI: C1541333
Disease: adult acute myeloid leukemia with inv(16)(p13;q22)
adult acute myeloid leukemia with inv(16)(p13;q22) 		1 0 1 0.12 0 0