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: C2931246
Disease: Potocki-Lupski syndrome
Potocki-Lupski syndrome 		7 0 6 0.12 0 0
CUI: C4684942
Disease: Refractory Thyroid Gland Carcinoma
Refractory Thyroid Gland Carcinoma 		10 0 5 9.6E-02 0 0
CUI: C4021631
Disease: Abnormal tracheobronchial morphology
Abnormal tracheobronchial morphology 		4 0 4 8.5E-02 0 0
CUI: C1282979
Disease: Transient hypoparathyroidism
Transient hypoparathyroidism 		5 0 4 8.3E-02 0 0
CUI: C1844007
Disease: Corticospinal tract hypoplasia
Corticospinal tract hypoplasia 		5 0 4 8.3E-02 0 0
CUI: C0577573
Disease: Mass of body region
Mass of body region 		22 0 5 7.8E-02 0 0
CUI: C0393814
Disease: Hereditary liability to pressure palsies
Hereditary liability to pressure palsies 		23 0 5 7.7E-02 0 0
CUI: C2748652
Disease: Large face
Large face 		11 0 4 7.4E-02 0 0
CUI: C0242621
Disease: Isochromosomes
Isochromosomes 		75 0 8 7.0E-02 0 0
CUI: C1849538
Disease: Delayed eruption of primary teeth
Delayed eruption of primary teeth 		14 0 4 7.0E-02 0 0
CUI: C3178806
Disease: Right Atrial Isomerism
Right Atrial Isomerism 		14 0 4 7.0E-02 0 0
CUI: C0751772
Disease: REM Sleep Behavior Disorder
REM Sleep Behavior Disorder 		46 0 6 6.9E-02 0 0
CUI: C1840382
Disease: Abnormality of the ureter
Abnormality of the ureter 		19 0 4 6.5E-02 0 0
CUI: C0034880
Disease: Hyperacusis
Hyperacusis 		20 0 4 6.3E-02 0 0
CUI: C0040156
Disease: Thyrotoxicosis
Thyrotoxicosis 		37 0 5 6.3E-02 0 0
CUI: C0085271
Disease: Self-Injurious Behavior
Self-Injurious Behavior 		91 0 8 6.2E-02 0 0
CUI: C0008733
Disease: Chylothorax
Chylothorax 		23 0 4 6.1E-02 0 0
CUI: C0432254
Disease: Singleton Merten syndrome
Singleton Merten syndrome 		8 1 3 5.8E-02 1 0.12
CUI: C1709457
Disease: Papillary Thyroid Microcarcinoma
Papillary Thyroid Microcarcinoma 		46 0 5 5.7E-02 0 0
CUI: C0085292
Disease: Stiff-Person Syndrome
Stiff-Person Syndrome 		34 0 4 5.2E-02 0 0
CUI: C4021753
Disease: Abnormality of the immune system
Abnormality of the immune system 		34 0 4 5.2E-02 0 0
CUI: C1853490
Disease: 22q13.3 Deletion Syndrome
22q13.3 Deletion Syndrome 		15 0 3 5.1E-02 0 0
CUI: C1839767
Disease: Tented upper lip vermilion
Tented upper lip vermilion 		79 0 6 5.0E-02 0 0
CUI: C0266039
Disease: Taurodontism
Taurodontism 		40 0 4 4.8E-02 0 0
CUI: C4020968
Disease: Abnormal localization of kidney
Abnormal localization of kidney 		40 0 4 4.8E-02 0 0