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: C0043345
Disease: Xeroderma
Xeroderma 		0 1 0 0 1 2.5E-02
CUI: C0241237
Disease: Difficulty standing
Difficulty standing 		0 14 0 0 1 1.9E-02
CUI: C0393907
Disease: Axonal sensorimotor neuropathy
Axonal sensorimotor neuropathy 		0 2 0 0 1 2.4E-02
CUI: C0432562
Disease: Malignant lymphoma of spleen
Malignant lymphoma of spleen 		0 2 0 0 2 5.0E-02
CUI: C1827841
Disease: Enzyme activity finding
Enzyme activity finding 		0 2 0 0 2 5.0E-02
CUI: C1840169
Disease: CORONARY ARTERY DISEASE, SUSCEPTIBILITY TO
CORONARY ARTERY DISEASE, SUSCEPTIBILITY TO 		0 3 0 0 2 4.9E-02
CUI: C1842247
Disease: CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1 		0 35 0 0 1 1.4E-02
CUI: C1845155
Disease: Exercise-induced myoglobinuria
Exercise-induced myoglobinuria 		0 2 0 0 1 2.4E-02
CUI: C1846672
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I 		0 52 0 0 1 1.1E-02
CUI: C1847759
Disease: MUSCULAR DYSTROPHY, CONGENITAL, 1C
MUSCULAR DYSTROPHY, CONGENITAL, 1C 		0 12 0 0 1 2.0E-02
CUI: C1868595
Disease: PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder)
PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder) 		0 5 0 0 1 2.3E-02
CUI: C2674665
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 5 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 5 (finding) 		0 1 0 0 1 2.5E-02
CUI: C3149706
Disease: CORONARY ARTERY SPASM 2, SUSCEPTIBILITY TO
CORONARY ARTERY SPASM 2, SUSCEPTIBILITY TO 		0 1 0 0 1 2.5E-02
CUI: C3150413
Disease: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 		0 7 0 0 1 2.2E-02
CUI: C3160761
Disease: Diabetic dyslipidaemia
Diabetic dyslipidaemia 		0 11 0 0 1 2.0E-02
CUI: C4024883
Disease: Hyperextensible skin of face
Hyperextensible skin of face 		0 2 0 0 1 2.4E-02
CUI: C4284790
Disease: Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies) Type A, 1
Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies) Type A, 1 		0 16 0 0 1 1.8E-02
CUI: C1854882
Disease: Absent speech
Absent speech 		232 0 1 1.6E-03 0 0
CUI: C0266483
Disease: Pachygyria
Pachygyria 		129 0 1 2.0E-03 0 0
CUI: C0014877
Disease: Esotropia
Esotropia 		121 0 1 2.0E-03 0 0
CUI: C0162701
Disease: Polysomnography
Polysomnography 		119 0 1 2.0E-03 0 0
CUI: C1837658
Disease: Gross motor development delay
Gross motor development delay 		118 0 1 2.0E-03 0 0
CUI: C1277241
Disease: Delayed myelination
Delayed myelination 		112 0 1 2.0E-03 0 0
CUI: C3161330
Disease: Profound intellectual disabilities
Profound intellectual disabilities 		112 0 1 2.0E-03 0 0
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		104 0 1 2.1E-03 0 0