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: C4025515
Disease: Cortical subperiosteal resorption of humeral metaphyses
Cortical subperiosteal resorption of humeral metaphyses 		2 0 2 0.11 0 0
CUI: C1864100
Disease: PSEUDOHYPOPARATHYROIDISM, TYPE IB
PSEUDOHYPOPARATHYROIDISM, TYPE IB 		13 0 3 0.10 0 0
CUI: C0151940
Disease: Hypocalcemic tetany
Hypocalcemic tetany 		4 0 2 9.5E-02 0 0
CUI: C0220983
Disease: Metabolic alkalosis
Metabolic alkalosis 		27 5 4 9.5E-02 1 0.14
CUI: C0342198
Disease: Thyrotoxicosis due to pituitary thyroid hormone resistance
Thyrotoxicosis due to pituitary thyroid hormone resistance 		4 0 2 9.5E-02 0 0
CUI: C0239134
Disease: Productive Cough
Productive Cough 		17 0 3 9.1E-02 0 0
CUI: C0740651
Disease: Abdominal symptom
Abdominal symptom 		17 0 3 9.1E-02 0 0
CUI: C4552938
Disease: Productive Cough, CTCAE
Productive Cough, CTCAE 		17 0 3 9.1E-02 0 0
CUI: C3494506
Disease: Pseudohypoparathyroidism, Type Ia
Pseudohypoparathyroidism, Type Ia 		30 0 4 8.9E-02 0 0
CUI: C0020595
Disease: Hypoaldosteronism
Hypoaldosteronism 		18 0 3 8.8E-02 0 0
CUI: C0857973
Disease: Elevated circulating parathyroid hormone level
Elevated circulating parathyroid hormone level 		18 0 3 8.8E-02 0 0
CUI: C3838731
Disease: Familial hyperaldosteronism type 1
Familial hyperaldosteronism type 1 		6 0 2 8.7E-02 0 0
CUI: C4551853
Disease: Diaphyseal sclerosis
Diaphyseal sclerosis 		6 0 2 8.7E-02 0 0
CUI: C0238015
Disease: Autonomic Dysreflexia
Autonomic Dysreflexia 		7 0 2 8.3E-02 0 0
CUI: C0598428
Disease: genetic hypertension
genetic hypertension 		34 0 4 8.2E-02 0 0
CUI: C0339985
Disease: Idiopathic bronchiectasis
Idiopathic bronchiectasis 		21 0 3 8.1E-02 0 0
CUI: C0342488
Disease: Mineralocorticoid Excess Syndrome, Apparent
Mineralocorticoid Excess Syndrome, Apparent 		8 0 2 8.0E-02 0 0
CUI: C0268790
Disease: Renal vascular disorder
Renal vascular disorder 		22 0 3 7.9E-02 0 0
CUI: C2931404
Disease: Albright's hereditary osteodystrophy
Albright's hereditary osteodystrophy 		22 0 3 7.9E-02 0 0
CUI: C0034642
Disease: Rales
Rales 		23 0 3 7.7E-02 0 0
CUI: C1843366
Disease: NIEMANN-PICK DISEASE, TYPE C2
NIEMANN-PICK DISEASE, TYPE C2 		9 0 2 7.7E-02 0 0
CUI: C3163798
Disease: Recurrent lower respiratory tract infection
Recurrent lower respiratory tract infection 		23 0 3 7.7E-02 0 0
CUI: C4324685
Disease: Hypertensive end-organ damage
Hypertensive end-organ damage 		9 0 2 7.7E-02 0 0
CUI: C4684865
Disease: Cerebral Adrenoleukodystrophy
Cerebral Adrenoleukodystrophy 		9 0 2 7.7E-02 0 0
CUI: C0235063
Disease: Respiratory Depression
Respiratory Depression 		24 0 3 7.5E-02 0 0