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: C0221154
Disease: Paroxysmal hypertension
Paroxysmal hypertension 		9 0 2 0.11 0 0
CUI: C0345832
Disease: Neoplasm of small intestine
Neoplasm of small intestine 		9 0 2 0.11 0 0
CUI: C0521670
Disease: Cranial nerve compression
Cranial nerve compression 		19 0 3 0.11 0 0
CUI: C1333944
Disease: Paraganglioma of head and neck
Paraganglioma of head and neck 		19 0 3 0.11 0 0
CUI: C1533847
Disease: Disorder of skeletal muscle
Disorder of skeletal muscle 		29 0 4 0.11 0 0
CUI: C2216370
Disease: Cherry red spot of the macula
Cherry red spot of the macula 		9 0 2 0.11 0 0
CUI: C0454641
Disease: Expressive language delay
Expressive language delay 		30 0 4 0.11 0 0
CUI: C1857171
Disease: Episodic hyperhidrosis
Episodic hyperhidrosis 		20 0 3 0.11 0 0
CUI: C2930839
Disease: Bilateral pheochromocytoma and islet cell adenoma of the pancreas
Bilateral pheochromocytoma and islet cell adenoma of the pancreas 		10 0 2 0.11 0 0
CUI: C3697716
Disease: Acute flaccid paralysis
Acute flaccid paralysis 		10 0 2 0.11 0 0
CUI: C4021849
Disease: Conjunctival hamartoma
Conjunctival hamartoma 		10 0 2 0.11 0 0
CUI: C0036161
Disease: Sandhoff Disease
Sandhoff Disease 		21 0 3 0.10 0 0
CUI: C1846176
Disease: Hyperactive deep tendon reflexes
Hyperactive deep tendon reflexes 		32 0 4 0.10 0 0
CUI: C0751559
Disease: Pulsatile Tinnitus
Pulsatile Tinnitus 		23 0 3 9.7E-02 0 0
CUI: C1708353
Disease: Hereditary Paraganglioma-Pheochromocytoma Syndrome
Hereditary Paraganglioma-Pheochromocytoma Syndrome 		23 0 3 9.7E-02 0 0
CUI: C1859736
Disease: Progressive spastic quadriplegia
Progressive spastic quadriplegia 		12 0 2 9.5E-02 0 0
CUI: C0152132
Disease: Hypertensive Retinopathy
Hypertensive Retinopathy 		24 0 3 9.4E-02 0 0
CUI: C0221069
Disease: Anterior Spinal Artery Syndrome
Anterior Spinal Artery Syndrome 		1 0 1 9.1E-02 0 0
CUI: C0268262
Disease: Metachromatic Leukodystrophy due to Saposin B Deficiency
Metachromatic Leukodystrophy due to Saposin B Deficiency 		1 0 1 9.1E-02 0 0
CUI: C0392322
Disease: Undifferentiated schizophrenia
Undifferentiated schizophrenia 		1 0 1 9.1E-02 0 0
CUI: C0393560
Disease: Vascular Dementia, Acute Onset
Vascular Dementia, Acute Onset 		1 0 1 9.1E-02 0 0
CUI: C0401067
Disease: Unilateral inguinal hernia NOS
Unilateral inguinal hernia NOS 		1 0 1 9.1E-02 0 0
CUI: C0423640
Disease: Right Flank Pain
Right Flank Pain 		1 0 1 9.1E-02 0 0
CUI: C0520559
Disease: Numbness of tongue
Numbness of tongue 		1 0 1 9.1E-02 0 0
CUI: C0521527
Disease: Shortened trunk
Shortened trunk 		1 0 1 9.1E-02 0 0