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: C0685409
Disease: Congenital Camptodactyly
Congenital Camptodactyly 		112 0 1 8.9E-03 0 0
CUI: C0836924
Disease: Thrombocytosis
Thrombocytosis 		29 0 1 3.4E-02 0 0
CUI: C0848558
Disease: Hypospadias
Hypospadias 		266 0 1 3.8E-03 0 0
CUI: C0855997
Disease: Abnormal basophil morphology
Abnormal basophil morphology 		3 0 1 0.33 0 0
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		593 0 1 1.7E-03 0 0
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: C1839798
Disease: Long nose
Long nose 		29 0 1 3.4E-02 0 0
CUI: C1844505
Disease: Pointed chin
Pointed chin 		71 0 1 1.4E-02 0 0
CUI: C1844592
Disease: Soft skin
Soft skin 		22 0 1 4.5E-02 0 0
CUI: C1849089
Disease: Broad forehead
Broad forehead 		133 0 1 7.5E-03 0 0
CUI: C1850780
Disease: Reduced leukocyte alkaline phosphatase
Reduced leukocyte alkaline phosphatase 		2 0 1 0.50 0 0
CUI: C1851835
Disease: Narrow maxilla
Narrow maxilla 		3 0 1 0.33 0 0
CUI: C1854114
Disease: Short nose
Short nose 		265 0 1 3.8E-03 0 0
CUI: C1855472
Disease: Acute lymphoblastic leukemia with lymphomatous features
Acute lymphoblastic leukemia with lymphomatous features 		6 0 1 0.17 0 0
CUI: C2919142
Disease: Short Stature, CTCAE
Short Stature, CTCAE 		1005 0 1 1.0E-03 0 0
CUI: C3697248
Disease: Short lower third of face
Short lower third of face 		33 0 1 3.0E-02 0 0
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: C4317152
Disease: Dimple chin
Dimple chin 		16 2 1 6.2E-02 1 0.33
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: C0032326
Disease: Pneumothorax
Pneumothorax 		30 3 1 3.3E-02 1 0.25
CUI: C0423757
Disease: Thin skin
Thin skin 		77 4 1 1.3E-02 1 0.20
CUI: C1856121
Disease: Broad eyebrow
Broad eyebrow 		11 4 1 9.1E-02 1 0.20
CUI: C1866806
Disease: Unilateral ptosis
Unilateral ptosis 		6 4 1 0.17 1 0.20
CUI: C0003466
Disease: Anus, Imperforate
Anus, Imperforate 		121 8 1 8.3E-03 1 0.11