Source: INFERRED ×
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: C4016396
Disease: LEUKEMIA, PHILADELPHIA CHROMOSOME-POSITIVE, RESISTANT TO IMATINIB
LEUKEMIA, PHILADELPHIA CHROMOSOME-POSITIVE, RESISTANT TO IMATINIB 		1 0 1 1.00 0 0
CUI: C4023165
Disease: Abnormality of skeletal morphology
Abnormality of skeletal morphology 		1 2 1 1.00 2 1.00
CUI: C4539857
Disease: CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME
CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME 		1 2 1 1.00 2 1.00
CUI: C1709527
Disease: B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1
B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1 		2 0 1 0.50 0 0
CUI: C1850780
Disease: Reduced leukocyte alkaline phosphatase
Reduced leukocyte alkaline phosphatase 		2 0 1 0.50 0 0
CUI: C0855997
Disease: Abnormal basophil morphology
Abnormal basophil morphology 		3 0 1 0.33 0 0
CUI: C1851835
Disease: Narrow maxilla
Narrow maxilla 		3 0 1 0.33 0 0
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease 		6 33 1 0.17 2 6.1E-02
CUI: C1855472
Disease: Acute lymphoblastic leukemia with lymphomatous features
Acute lymphoblastic leukemia with lymphomatous features 		6 0 1 0.17 0 0
CUI: C1866806
Disease: Unilateral ptosis
Unilateral ptosis 		6 4 1 0.17 1 0.20
CUI: C1856121
Disease: Broad eyebrow
Broad eyebrow 		11 4 1 9.1E-02 1 0.20
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
Myeloid Leukemia, Chronic 		13 0 1 7.7E-02 0 0
CUI: C0027022
Disease: Myeloproliferative disease
Myeloproliferative disease 		15 0 1 6.7E-02 0 0
CUI: C4317152
Disease: Dimple chin
Dimple chin 		16 2 1 6.2E-02 1 0.33
CUI: C0426422
Disease: Narrow nose
Narrow nose 		17 0 1 5.9E-02 0 0
CUI: C1844592
Disease: Soft skin
Soft skin 		22 0 1 4.5E-02 0 0
CUI: C0836924
Disease: Thrombocytosis
Thrombocytosis 		29 0 1 3.4E-02 0 0
CUI: C1839798
Disease: Long nose
Long nose 		29 0 1 3.4E-02 0 0
CUI: C0032326
Disease: Pneumothorax
Pneumothorax 		30 3 1 3.3E-02 1 0.25
CUI: C0232462
Disease: Decrease in appetite
Decrease in appetite 		33 0 1 3.0E-02 0 0
CUI: C3697248
Disease: Short lower third of face
Short lower third of face 		33 0 1 3.0E-02 0 0
CUI: C1386048
Disease: Intrauterine retardation
Intrauterine retardation 		41 56 1 2.4E-02 1 1.8E-02
CUI: C0023518
Disease: Leukocytosis
Leukocytosis 		51 0 1 2.0E-02 0 0
CUI: C1844505
Disease: Pointed chin
Pointed chin 		71 0 1 1.4E-02 0 0
CUI: C0263401
Disease: Cutis marmorata
Cutis marmorata 		77 9 1 1.3E-02 1 1.0E-01