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: C1856697
Disease: Mitochondrial malic enzyme reduced
Mitochondrial malic enzyme reduced 		1 0 1 0.33 0 0
CUI: C3277918
Disease: TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 1
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 1 		1 0 1 0.33 0 0
CUI: C3889615
Disease: TRANSFERRIN VARIANT D1 PHENOTYPE
TRANSFERRIN VARIANT D1 PHENOTYPE 		1 0 1 0.33 0 0
CUI: C3889617
Disease: TRANSFERRIN VARIANT B2 PHENOTYPE
TRANSFERRIN VARIANT B2 PHENOTYPE 		1 0 1 0.33 0 0
CUI: C3889619
Disease: TRANSFERRIN VARIANT Bv PHENOTYPE
TRANSFERRIN VARIANT Bv PHENOTYPE 		1 0 1 0.33 0 0
CUI: C4021047
Disease: Impaired visually enhanced vestibulo-ocular reflex
Impaired visually enhanced vestibulo-ocular reflex 		1 0 1 0.33 0 0
CUI: C4025641
Disease: Decreased pyruvate carboxylase activity
Decreased pyruvate carboxylase activity 		1 0 1 0.33 0 0
CUI: C4225610
Disease: TRANSFERRIN VARIANT D(CHI)
TRANSFERRIN VARIANT D(CHI) 		1 0 1 0.33 0 0
CUI: C0202105
Disease: Transferrin measurement
Transferrin measurement 		6 0 2 0.29 0 0
CUI: C0428545
Disease: Serum transferrin measurement
Serum transferrin measurement 		6 0 2 0.29 0 0
CUI: C0393520
Disease: Harding ataxia
Harding ataxia 		2 0 1 0.25 0 0
CUI: C0742191
Disease: Cervical spinal cord atrophy
Cervical spinal cord atrophy 		2 0 1 0.25 0 0
CUI: C0393578
Disease: Pallidoluysian degeneration
Pallidoluysian degeneration 		3 0 1 0.20 0 0
CUI: C0476369
Disease: Echocardiogram abnormal
Echocardiogram abnormal 		3 0 1 0.20 0 0
CUI: C4024943
Disease: Decreased amplitude of sensory action potentials
Decreased amplitude of sensory action potentials 		3 0 1 0.20 0 0
CUI: C4518339
Disease: Sporadic adult-onset ataxia of unknown etiology
Sporadic adult-onset ataxia of unknown etiology 		3 0 1 0.20 0 0
CUI: C1395088
Disease: Nervous system--Degeneration
Nervous system--Degeneration 		4 0 1 0.17 0 0
CUI: C0342784
Disease: Pearson's marrow-pancreas syndrome
Pearson's marrow-pancreas syndrome 		5 0 1 0.14 0 0
CUI: C3711370
Disease: Spastic Paraplegia Type 7
Spastic Paraplegia Type 7 		5 0 1 0.14 0 0
CUI: C4275170
Disease: Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1
Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 		5 0 1 0.14 0 0
CUI: C0001308
Disease: Acute and subacute liver necrosis (disorder)
Acute and subacute liver necrosis (disorder) 		6 0 1 0.12 0 0
CUI: C0042875
Disease: Vitamin E Deficiency
Vitamin E Deficiency 		6 0 1 0.12 0 0
CUI: C3273225
Disease: Hereditary Neurodegenerative Disorder
Hereditary Neurodegenerative Disorder 		6 0 1 0.12 0 0
CUI: C0393807
Disease: Hereditary motor and sensory neuropathy with optic atrophy (disorder)
Hereditary motor and sensory neuropathy with optic atrophy (disorder) 		7 0 1 0.11 0 0
CUI: C1838027
Disease: Incomprehensible speech
Incomprehensible speech 		7 0 1 0.11 0 0