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: C0242339
Disease: Dyslipidemias
Dyslipidemias 		0 184 0 0 1 5.1E-03
CUI: C0242036
Disease: Paraplegia, Ataxic
Paraplegia, Ataxic 		1 0 1 7.1E-02 0 0
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis 		1 0 1 7.1E-02 0 0
CUI: C0271848
Disease: Hyperparathyroidism due to vitamin D deficiency
Hyperparathyroidism due to vitamin D deficiency 		1 0 1 7.1E-02 0 0
CUI: C0278114
Disease: Paraplegia, Cerebral
Paraplegia, Cerebral 		1 0 1 7.1E-02 0 0
CUI: C0278115
Disease: Paraplegia, Spinal
Paraplegia, Spinal 		1 0 1 7.1E-02 0 0
CUI: C0332977
Disease: Congenital hemangiomatosis
Congenital hemangiomatosis 		1 0 1 7.1E-02 0 0
CUI: C0342841
Disease: Hunter's syndrome, severe form
Hunter's syndrome, severe form 		1 0 1 7.1E-02 0 0
CUI: C0342842
Disease: Hunter's syndrome, mild form
Hunter's syndrome, mild form 		1 0 1 7.1E-02 0 0
CUI: C0346405
Disease: Ectopic parathyroid adenoma
Ectopic parathyroid adenoma 		1 0 1 7.1E-02 0 0
CUI: C0346408
Disease: Parathyroid hormone-related peptide-secreting tumor
Parathyroid hormone-related peptide-secreting tumor 		1 0 1 7.1E-02 0 0
CUI: C0393745
Disease: Chronic post-traumatic headache
Chronic post-traumatic headache 		1 0 1 7.1E-02 0 0
CUI: C0452143
Disease: Paraplegia, Flaccid
Paraplegia, Flaccid 		1 0 1 7.1E-02 0 0
CUI: C0456126
Disease: Neonatal rickets
Neonatal rickets 		1 0 1 7.1E-02 0 0
CUI: C0475187
Disease: Brown tumor of hyperparathyroidism
Brown tumor of hyperparathyroidism 		1 0 1 7.1E-02 0 0
CUI: C0477680
Disease: Adult osteomalacia, unspecified
Adult osteomalacia, unspecified 		1 0 1 7.1E-02 0 0
CUI: C0595928
Disease: Serum calcium increased
Serum calcium increased 		1 0 1 7.1E-02 0 0
CUI: C1300287
Disease: Transient neonatal hyperparathyroidism
Transient neonatal hyperparathyroidism 		1 0 1 7.1E-02 0 0
CUI: C1737223
Disease: Secondary hypoparathyroidism
Secondary hypoparathyroidism 		1 0 1 7.1E-02 0 0
CUI: C1820738
Disease: Feeding intolerance
Feeding intolerance 		1 1 1 7.1E-02 1 7.1E-02
CUI: C1832612
Disease: Hypocalcemia, Autosomal Dominant, with Bartter Syndrome
Hypocalcemia, Autosomal Dominant, with Bartter Syndrome 		1 0 1 7.1E-02 0 0
CUI: C1834421
Disease: Myxoid subcutaneous tumors
Myxoid subcutaneous tumors 		1 0 1 7.1E-02 0 0
CUI: C1840347
Disease: HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II (disorder)
HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II (disorder) 		1 0 1 7.1E-02 0 0
CUI: C1850635
Disease: Atrial myxoma, familial
Atrial myxoma, familial 		1 0 1 7.1E-02 0 0
CUI: C1851697
Disease: Pancreatic islet cell adenoma
Pancreatic islet cell adenoma 		1 0 1 7.1E-02 0 0