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: C0265202
Disease: Seckel syndrome
Seckel syndrome 		56 0 9 0.10 0 0
CUI: C4020962
Disease: Enlarged thorax
Enlarged thorax 		25 0 6 9.8E-02 0 0
CUI: C0265306
Disease: Greig cephalopolysyndactyly syndrome
Greig cephalopolysyndactyly syndrome 		14 0 5 9.8E-02 0 0
CUI: C4025749
Disease: Abnormality of the spleen
Abnormality of the spleen 		26 0 6 9.7E-02 0 0
CUI: C1275081
Disease: Cardio-facio-cutaneous syndrome
Cardio-facio-cutaneous syndrome 		28 0 6 9.4E-02 0 0
CUI: C0405580
Disease: Adrenal cortical hypofunction
Adrenal cortical hypofunction 		52 0 8 9.3E-02 0 0
CUI: C4023397
Disease: Abnormal hair quantity
Abnormal hair quantity 		29 0 6 9.2E-02 0 0
CUI: C4024878
Disease: Generalized hyperpigmentation
Generalized hyperpigmentation 		42 0 7 9.1E-02 0 0
CUI: C0175693
Disease: Russell-Silver syndrome
Russell-Silver syndrome 		104 0 12 9.0E-02 0 0
CUI: C0020617
Disease: Hypoglycemic coma
Hypoglycemic coma 		19 0 5 8.9E-02 0 0
CUI: C0020461
Disease: Hyperkalemia
Hyperkalemia 		32 0 6 8.8E-02 0 0
CUI: C4023909
Disease: Aplasia/Hypoplasia of the abdominal wall musculature
Aplasia/Hypoplasia of the abdominal wall musculature 		32 0 6 8.8E-02 0 0
CUI: C4284088
Disease: MIRAGE SYNDROME
MIRAGE SYNDROME 		8 0 4 8.7E-02 0 0
CUI: C0024236
Disease: Lymphedema
Lymphedema 		61 0 8 8.4E-02 0 0
CUI: C0238397
Disease: Pulmonary artery stenosis
Pulmonary artery stenosis 		36 0 6 8.3E-02 0 0
CUI: C4551602
Disease: Noonan Syndrome 1
Noonan Syndrome 1 		23 0 5 8.3E-02 0 0
CUI: C1837732
Disease: Thickened helices
Thickened helices 		37 0 6 8.2E-02 0 0
CUI: C0001623
Disease: Adrenal gland hypofunction
Adrenal gland hypofunction 		90 0 10 8.2E-02 0 0
CUI: C0558165
Disease: Curly hair (finding)
Curly hair (finding) 		24 0 5 8.2E-02 0 0
CUI: C0041409
Disease: Turner Syndrome, Male
Turner Syndrome, Male 		11 0 4 8.2E-02 0 0
CUI: C1527404
Disease: Female Pseudo-Turner Syndrome
Female Pseudo-Turner Syndrome 		11 0 4 8.2E-02 0 0
CUI: C1860991
Disease: NOONAN SYNDROME 3
NOONAN SYNDROME 3 		11 0 4 8.2E-02 0 0
CUI: C3164374
Disease: Abnormality of pulmonary valve
Abnormality of pulmonary valve 		40 0 6 7.9E-02 0 0
CUI: C1328931
Disease: Multiple lentigines
Multiple lentigines 		13 0 4 7.8E-02 0 0
CUI: C0009207
Disease: Cockayne Syndrome
Cockayne Syndrome 		85 0 9 7.6E-02 0 0