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: C0231246
Disease: Failure to gain weight
Failure to gain weight 		1 0 1 6.2E-02 0 0
CUI: C0575518
Disease: Hypertrophy of upper limb
Hypertrophy of upper limb 		1 0 1 6.2E-02 0 0
CUI: C1968811
Disease: Prominent antitragus
Prominent antitragus 		1 0 1 6.2E-02 0 0
CUI: C1968814
Disease: Slender ulna
Slender ulna 		1 0 1 6.2E-02 0 0
CUI: C3280203
Disease: WARBURG MICRO SYNDROME 3
WARBURG MICRO SYNDROME 3 		1 0 1 6.2E-02 0 0
CUI: C3280214
Disease: WARBURG MICRO SYNDROME 2
WARBURG MICRO SYNDROME 2 		1 0 1 6.2E-02 0 0
CUI: C3665817
Disease: Hypocarnitinaemia
Hypocarnitinaemia 		1 0 1 6.2E-02 0 0
CUI: C3806285
Disease: Recurrent infections due to aspiration
Recurrent infections due to aspiration 		1 0 1 6.2E-02 0 0
CUI: C3806286
Disease: Decreased sensitivity to hypoxemia
Decreased sensitivity to hypoxemia 		1 0 1 6.2E-02 0 0
CUI: C3810265
Disease: WARBURG MICRO SYNDROME 4
WARBURG MICRO SYNDROME 4 		1 0 1 6.2E-02 0 0
CUI: C4016396
Disease: LEUKEMIA, PHILADELPHIA CHROMOSOME-POSITIVE, RESISTANT TO IMATINIB
LEUKEMIA, PHILADELPHIA CHROMOSOME-POSITIVE, RESISTANT TO IMATINIB 		1 0 1 6.2E-02 0 0
CUI: C4023165
Disease: Abnormality of skeletal morphology
Abnormality of skeletal morphology 		1 0 1 6.2E-02 0 0
CUI: C4023803
Disease: Hypertrophy of the lower limb
Hypertrophy of the lower limb 		1 0 1 6.2E-02 0 0
CUI: C4288091
Disease: Tubulocystic renal cell carcinoma
Tubulocystic renal cell carcinoma 		1 0 1 6.2E-02 0 0
CUI: C4539857
Disease: CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME
CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME 		1 0 1 6.2E-02 0 0
CUI: C0432066
Disease: Congenital malformation syndromes affecting facial appearance
Congenital malformation syndromes affecting facial appearance 		2 0 2 0.12 0 0
CUI: C0544669
Disease: Hypomanic personality
Hypomanic personality 		2 0 1 5.9E-02 0 0
CUI: C0555970
Disease: Nasal infection
Nasal infection 		2 0 1 5.9E-02 0 0
CUI: C0920187
Disease: Congenital neuropathy
Congenital neuropathy 		2 0 1 5.9E-02 0 0
CUI: C1283620
Disease: Sucrase-isomaltase deficiency, congenital
Sucrase-isomaltase deficiency, congenital 		2 0 1 5.9E-02 0 0
CUI: C1850780
Disease: Reduced leukocyte alkaline phosphatase
Reduced leukocyte alkaline phosphatase 		2 0 1 5.9E-02 0 0
CUI: C1855513
Disease: Prominent nipples
Prominent nipples 		2 0 1 5.9E-02 0 0
CUI: C2675370
Disease: Capillary Malformation Without Arteriovenous Malformation
Capillary Malformation Without Arteriovenous Malformation 		2 0 1 5.9E-02 0 0
CUI: C3275453
Disease: Cutaneous capillary malformation
Cutaneous capillary malformation 		2 0 1 5.9E-02 0 0
CUI: C4025740
Disease: Autoamputation of foot
Autoamputation of foot 		2 0 1 5.9E-02 0 0