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: C3241937
Disease: Nonalcoholic Steatohepatitis
Nonalcoholic Steatohepatitis 		0 17 0 0 1 1.1E-02
CUI: C0202115
Disease: Lactic acid measurement
Lactic acid measurement 		1 0 1 4.3E-02 0 0
CUI: C0394004
Disease: Congenital non-progressive ataxia
Congenital non-progressive ataxia 		1 0 1 4.3E-02 0 0
CUI: C0475733
Disease: Idiopathic infantile hypercalcemia - mild form
Idiopathic infantile hypercalcemia - mild form 		1 0 1 4.3E-02 0 0
CUI: C0595928
Disease: Serum calcium increased
Serum calcium increased 		1 0 1 4.3E-02 0 0
CUI: C0810006
Disease: Acute cerebrovascular disease
Acute cerebrovascular disease 		1 0 1 4.3E-02 0 0
CUI: C0858233
Disease: Stridor, Congenital
Stridor, Congenital 		1 0 1 4.3E-02 0 0
CUI: C1820738
Disease: Feeding intolerance
Feeding intolerance 		1 0 1 4.3E-02 0 0
CUI: C1832612
Disease: Hypocalcemia, Autosomal Dominant, with Bartter Syndrome
Hypocalcemia, Autosomal Dominant, with Bartter Syndrome 		1 0 1 4.3E-02 0 0
CUI: C1842797
Disease: Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like
Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like 		1 0 1 4.3E-02 0 0
CUI: C1847725
Disease: SPINOCEREBELLAR ATAXIA 15
SPINOCEREBELLAR ATAXIA 15 		1 0 1 4.3E-02 0 0
CUI: C1851095
Disease: Lumbosacral hirsutism
Lumbosacral hirsutism 		1 0 1 4.3E-02 0 0
CUI: C1857787
Disease: Aplasia of the inferior half of the cerebellar vermis
Aplasia of the inferior half of the cerebellar vermis 		1 0 1 4.3E-02 0 0
CUI: C2752062
Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 8
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 8 		1 0 1 4.3E-02 0 0
CUI: C3150714
Disease: FASTING PLASMA GLUCOSE LEVEL QUANTITATIVE TRAIT LOCUS 5
FASTING PLASMA GLUCOSE LEVEL QUANTITATIVE TRAIT LOCUS 5 		1 0 1 4.3E-02 0 0
CUI: C4021006
Disease: Short distal phalanx of the 5th toe
Short distal phalanx of the 5th toe 		1 0 1 4.3E-02 0 0
CUI: C4021280
Disease: Curved 4th toe phalanx
Curved 4th toe phalanx 		1 0 1 4.3E-02 0 0
CUI: C4225407
Disease: PEELING SKIN SYNDROME 4
PEELING SKIN SYNDROME 4 		1 0 1 4.3E-02 0 0
CUI: C4274322
Disease: Spinocerebellar ataxia type 15/16
Spinocerebellar ataxia type 15/16 		1 0 1 4.3E-02 0 0
CUI: C4304527
Disease: 6q25 microdeletion syndrome
6q25 microdeletion syndrome 		1 0 1 4.3E-02 0 0
CUI: C4551629
Disease: Congenital talipes calcaneovalgus
Congenital talipes calcaneovalgus 		1 0 1 4.3E-02 0 0
CUI: C4747885
Disease: HYDROCEPHALUS, CONGENITAL, 3, WITH BRAIN ANOMALIES
HYDROCEPHALUS, CONGENITAL, 3, WITH BRAIN ANOMALIES 		1 0 1 4.3E-02 0 0
CUI: C0003132
Disease: Anoxic Encephalopathy
Anoxic Encephalopathy 		2 0 1 4.2E-02 0 0
CUI: C0342639
Disease: Familial idiopathic hypercalciuria
Familial idiopathic hypercalciuria 		2 0 1 4.2E-02 0 0
CUI: C0345406
Disease: Neonatal hyperparathyroidism
Neonatal hyperparathyroidism 		2 0 1 4.2E-02 0 0