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: C1837761
Disease: Narrow nasal ridge
Narrow nasal ridge 		11 0 1 9.1E-02 0 0
CUI: C4014733
Disease: Follicular hyperplasia
Follicular hyperplasia 		11 0 1 9.1E-02 0 0
CUI: C4023551
Disease: Abnormality of dental color
Abnormality of dental color 		11 0 1 9.1E-02 0 0
CUI: C4551602
Disease: Noonan Syndrome 1
Noonan Syndrome 1 		11 73 1 9.1E-02 2 2.7E-02
CUI: C0028326
Disease: Noonan Syndrome
Noonan Syndrome 		12 153 1 8.3E-02 1 6.5E-03
CUI: C0263383
Disease: Keratosis pilaris
Keratosis pilaris 		12 0 1 8.3E-02 0 0
CUI: C1858033
Disease: Asymmetry of the thorax
Asymmetry of the thorax 		12 0 1 8.3E-02 0 0
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
Myeloid Leukemia, Chronic 		13 0 1 7.7E-02 0 0
CUI: C0206682
Disease: Follicular thyroid carcinoma
Follicular thyroid carcinoma 		14 0 1 7.1E-02 0 0
CUI: C0332890
Disease: Congenital hemihypertrophy
Congenital hemihypertrophy 		14 0 1 7.1E-02 0 0
CUI: C0431391
Disease: Hemimegalencephaly
Hemimegalencephaly 		14 0 1 7.1E-02 0 0
CUI: C1704375
Disease: Hypophosphatemic Rickets
Hypophosphatemic Rickets 		15 0 1 6.7E-02 0 0
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
Lymphoma, Non-Hodgkin, Familial 		15 33 1 6.7E-02 1 2.9E-02
CUI: C0280631
Disease: Leiomyosarcoma of uterus
Leiomyosarcoma of uterus 		16 0 1 6.2E-02 0 0
CUI: C4023385
Disease: Aplasia of the semicircular canal
Aplasia of the semicircular canal 		16 0 1 6.2E-02 0 0
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms 		17 0 1 5.9E-02 0 0
CUI: C0027439
Disease: Nasopharyngeal Neoplasms
Nasopharyngeal Neoplasms 		19 0 1 5.3E-02 0 0
CUI: C0035412
Disease: Rhabdomyosarcoma
Rhabdomyosarcoma 		19 0 1 5.3E-02 0 0
CUI: C0206686
Disease: Adrenocortical carcinoma
Adrenocortical carcinoma 		20 0 1 5.0E-02 0 0
CUI: C0265319
Disease: Fibrous skin tumor of tuberous sclerosis
Fibrous skin tumor of tuberous sclerosis 		20 0 1 5.0E-02 0 0
CUI: C0855740
Disease: Abnormal platelet function
Abnormal platelet function 		21 0 1 4.8E-02 0 0
CUI: C4024989
Disease: Hereditary nonpolyposis colorectal carcinoma
Hereditary nonpolyposis colorectal carcinoma 		21 0 1 4.8E-02 0 0
CUI: C0152235
Disease: Congenital genu recurvatum
Congenital genu recurvatum 		23 0 1 4.3E-02 0 0
CUI: C0158486
Disease: Acquired genu recurvatum
Acquired genu recurvatum 		23 0 1 4.3E-02 0 0
CUI: C0558165
Disease: Curly hair (finding)
Curly hair (finding) 		24 0 1 4.2E-02 0 0