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: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
ABLEPHARON-MACROSTOMIA SYNDROME 		41 0 1 2.1E-02 0 0
CUI: C0522216
Disease: Abnormal auditory evoked potential
Abnormal auditory evoked potential 		11 0 1 5.9E-02 0 0
CUI: C4021152
Disease: Abnormal CNS myelination
Abnormal CNS myelination 		9 0 1 6.7E-02 0 0
CUI: C1842581
Disease: Abnormal corpus callosum morphology
Abnormal corpus callosum morphology 		70 0 1 1.3E-02 0 0
CUI: C4025252
Disease: Abnormal nasal morphology
Abnormal nasal morphology 		34 0 4 0.11 0 0
CUI: C4025648
Disease: Abnormal peripheral myelination
Abnormal peripheral myelination 		2 0 1 0.12 0 0
CUI: C1260926
Disease: Abnormal pigmentation
Abnormal pigmentation 		58 0 1 1.6E-02 0 0
CUI: C0522214
Disease: Abnormal visual evoked potential
Abnormal visual evoked potential 		55 0 1 1.6E-02 0 0
CUI: C1328440
Disease: Abnormality of amino acid metabolism
Abnormality of amino acid metabolism 		8 0 3 0.25 0 0
CUI: C4023722
Disease: Abnormality of hair texture
Abnormality of hair texture 		15 0 1 4.8E-02 0 0
CUI: C4023616
Disease: Abnormality of immune system physiology
Abnormality of immune system physiology 		42 0 4 8.9E-02 0 0
CUI: C4025797
Disease: Abnormality of prenatal development or birth
Abnormality of prenatal development or birth 		23 0 2 7.1E-02 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		215 0 4 1.8E-02 0 0
CUI: C0262444
Disease: Abnormality of the dentition
Abnormality of the dentition 		140 0 3 2.1E-02 0 0
CUI: C0857379
Disease: Abnormality of the pinna
Abnormality of the pinna 		85 0 1 1.1E-02 0 0
CUI: C4021797
Disease: Abnormality of the thorax
Abnormality of the thorax 		40 0 1 2.2E-02 0 0
CUI: C0241267
Disease: Absence of subcutaneous fat
Absence of subcutaneous fat 		11 0 2 0.12 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex 		201 0 1 4.8E-03 0 0
CUI: C0221369
Disease: Acquired Camptodactyly
Acquired Camptodactyly 		120 0 1 7.9E-03 0 0
CUI: C0600033
Disease: Acquired Kyphoscoliosis
Acquired Kyphoscoliosis 		149 0 3 2.0E-02 0 0
CUI: C0022602
Disease: Actinic keratosis
Actinic keratosis 		136 0 1 7.0E-03 0 0
CUI: C0234376
Disease: Action Tremor
Action Tremor 		95 0 2 2.0E-02 0 0
CUI: C0085669
Disease: Acute leukemia
Acute leukemia 		639 0 1 1.6E-03 0 0
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia 		1293 0 2 1.5E-03 0 0
CUI: C0023465
Disease: Acute monocytic leukemia
Acute monocytic leukemia 		633 0 1 1.6E-03 0 0