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: C4304578
Disease: 1p21.3 microdeletion syndrome
1p21.3 microdeletion syndrome 		1 0 1 1.00 0 0
CUI: C0034139
Disease: Purine-Pyrimidine Metabolism, Inborn Errors
Purine-Pyrimidine Metabolism, Inborn Errors 		2 0 1 0.50 0 0
CUI: C0274576
Disease: Poisoning by fluorouracil
Poisoning by fluorouracil 		2 0 1 0.50 0 0
CUI: C0750325
Disease: Vomiting, recurrent
Vomiting, recurrent 		2 0 1 0.50 0 0
CUI: C4025582
Disease: Reduced dihydropyrimidine dehydrogenase activity
Reduced dihydropyrimidine dehydrogenase activity 		2 0 1 0.50 0 0
CUI: C0476270
Disease: Cardiovascular symptoms
Cardiovascular symptoms 		3 0 1 0.33 0 0
CUI: C1848657
Disease: Long ear
Long ear 		3 0 1 0.33 0 0
CUI: C3495551
Disease: Dihydropyrimidinuria
Dihydropyrimidinuria 		3 0 1 0.33 0 0
CUI: C4531196
Disease: Transthyretin cardiac amyloidosis
Transthyretin cardiac amyloidosis 		3 0 1 0.33 0 0
CUI: C0036224
Disease: Sarcoma, Yoshida
Sarcoma, Yoshida 		6 0 1 0.17 0 0
CUI: C0027660
Disease: Neoplasms, Glandular and Epithelial
Neoplasms, Glandular and Epithelial 		7 0 1 0.14 0 0
CUI: C1959620
Disease: Dihydropyrimidine Dehydrogenase Deficiency
Dihydropyrimidine Dehydrogenase Deficiency 		7 0 1 0.14 0 0
CUI: C0852711
Disease: Sickle Cell Dactylitis
Sickle Cell Dactylitis 		8 0 1 0.12 0 0
CUI: C4021982
Disease: Abnormal eating behavior
Abnormal eating behavior 		8 0 1 0.12 0 0
CUI: C0037020
Disease: Shyness
Shyness 		9 0 1 0.11 0 0
CUI: C0151773
Disease: Bone marrow depression
Bone marrow depression 		9 0 1 0.11 0 0
CUI: C0023012
Disease: Language Delay
Language Delay 		11 0 1 9.1E-02 0 0
CUI: C0454655
Disease: Semantic-Pragmatic Disorder
Semantic-Pragmatic Disorder 		11 0 1 9.1E-02 0 0
CUI: C0549410
Disease: Palmar-plantar erythrodysesthesia syndrome
Palmar-plantar erythrodysesthesia syndrome 		11 0 1 9.1E-02 0 0
CUI: C0677984
Disease: Locally Advanced Malignant Neoplasm
Locally Advanced Malignant Neoplasm 		11 0 1 9.1E-02 0 0
CUI: C0751257
Disease: Auditory Processing Disorder, Central
Auditory Processing Disorder, Central 		11 0 1 9.1E-02 0 0
CUI: C3714580
Disease: Hypokalemic periodic paralysis type 1
Hypokalemic periodic paralysis type 1 		12 0 1 8.3E-02 0 0
CUI: C0155502
Disease: Benign Paroxysmal Positional Vertigo
Benign Paroxysmal Positional Vertigo 		16 0 1 6.2E-02 0 0
CUI: C0278502
Disease: recurrent gastric cancer
recurrent gastric cancer 		16 0 1 6.2E-02 0 0
CUI: C0023014
Disease: Language Development Disorders
Language Development Disorders 		18 0 1 5.6E-02 0 0