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: C0796037
Disease: Martsolf syndrome
Martsolf syndrome 		6 0 6 0.38 0 0
CUI: C0406775
Disease: Symmetrical dyschromatosis of extremities
Symmetrical dyschromatosis of extremities 		22 0 7 0.23 0 0
CUI: C1833219
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B (disorder)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B (disorder) 		6 0 3 0.16 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: C1739405
Disease: CML progression
CML progression 		47 0 7 0.12 0 0
CUI: C0687154
Disease: Acrocephalopolysyndactyly
Acrocephalopolysyndactyly 		3 0 2 0.12 0 0
CUI: C1855772
Disease: Absent corpus callosum cataract immunodeficiency
Absent corpus callosum cataract immunodeficiency 		4 0 2 0.11 0 0
CUI: C1844527
Disease: Clitoral hypoplasia
Clitoral hypoplasia 		30 0 4 9.5E-02 0 0
CUI: C1849295
Disease: Hypoplastic labia minora
Hypoplastic labia minora 		30 0 4 9.5E-02 0 0
CUI: C0265233
Disease: Cryptophthalmos syndrome
Cryptophthalmos syndrome 		8 0 2 9.1E-02 0 0
CUI: C2936797
Disease: Acid cholesteryl ester hydrolase deficiency, type 2
Acid cholesteryl ester hydrolase deficiency, type 2 		9 0 2 8.7E-02 0 0
CUI: C0027889
Disease: Hereditary Sensory and Autonomic Neuropathies
Hereditary Sensory and Autonomic Neuropathies 		25 0 3 7.9E-02 0 0
CUI: C0035920
Disease: Rubella
Rubella 		82 0 7 7.7E-02 0 0
CUI: C4020968
Disease: Abnormal localization of kidney
Abnormal localization of kidney 		40 0 4 7.7E-02 0 0
CUI: C0221060
Disease: Mobius Syndrome
Mobius Syndrome 		28 0 3 7.3E-02 0 0
CUI: C0795878
Disease: Monosomy 22
Monosomy 22 		14 0 2 7.1E-02 0 0
CUI: C4288892
Disease: Infant Acute Undifferentiated Leukemia
Infant Acute Undifferentiated Leukemia 		14 0 2 7.1E-02 0 0
CUI: C4021395
Disease: Abnormality of the antihelix
Abnormality of the antihelix 		17 0 2 6.5E-02 0 0
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