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: C0553718
Disease: Renal artery occlusion
Renal artery occlusion 		3 0 1 5.6E-02 0 0
CUI: C1838063
Disease: Focal sensory auditory seizure
Focal sensory auditory seizure 		3 0 1 5.6E-02 0 0
CUI: C1848431
Disease: Xanthine nephrolithiasis
Xanthine nephrolithiasis 		3 0 1 5.6E-02 0 0
CUI: C1849128
Disease: Spastic paraplegia 15, autosomal recessive
Spastic paraplegia 15, autosomal recessive 		3 0 1 5.6E-02 0 0
CUI: C1863688
Disease: Xanthinuria, Type II
Xanthinuria, Type II 		3 0 1 5.6E-02 0 0
CUI: C2931355
Disease: Spastic paraplegia 3, autosomal dominant
Spastic paraplegia 3, autosomal dominant 		3 0 1 5.6E-02 0 0
CUI: C3811915
Disease: SUCLA2
SUCLA2 		3 0 1 5.6E-02 0 0
CUI: C4479278
Disease: AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS
AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS 		3 0 1 5.6E-02 0 0
CUI: C0007020
Disease: Carbon Monoxide Poisoning
Carbon Monoxide Poisoning 		4 0 1 5.3E-02 0 0
CUI: C0155300
Disease: Pseudopapilledema
Pseudopapilledema 		4 0 1 5.3E-02 0 0
CUI: C0234974
Disease: Simple Partial Seizures
Simple Partial Seizures 		4 0 1 5.3E-02 0 0
CUI: C0393738
Disease: Chronic tension-type headache
Chronic tension-type headache 		4 0 1 5.3E-02 0 0
CUI: C0855230
Disease: Food hoarding
Food hoarding 		4 0 1 5.3E-02 0 0
CUI: C1863052
Disease: ALZHEIMER DISEASE, FAMILIAL, 1
ALZHEIMER DISEASE, FAMILIAL, 1 		4 0 1 5.3E-02 0 0
CUI: C3150658
Disease: WARSAW BREAKAGE SYNDROME
WARSAW BREAKAGE SYNDROME 		4 0 1 5.3E-02 0 0
CUI: C4024970
Disease: Thick cerebral cortex
Thick cerebral cortex 		4 0 1 5.3E-02 0 0
CUI: C4274995
Disease: Lissencephaly with cerebellar hypoplasia
Lissencephaly with cerebellar hypoplasia 		4 0 1 5.3E-02 0 0
CUI: C4551895
Disease: Familial Cold Autoinflammatory Syndrome 1
Familial Cold Autoinflammatory Syndrome 1 		4 0 1 5.3E-02 0 0
CUI: C0011574
Disease: Involutional Depression
Involutional Depression 		25 0 2 5.1E-02 0 0
CUI: C1571983
Disease: Involutional paraphrenia
Involutional paraphrenia 		25 0 2 5.1E-02 0 0
CUI: C1571984
Disease: Psychosis, Involutional
Psychosis, Involutional 		25 0 2 5.1E-02 0 0
CUI: C0268118
Disease: Xanthinuria, Type I
Xanthinuria, Type I 		5 0 1 5.0E-02 0 0
CUI: C0271214
Disease: Central blindness
Central blindness 		5 0 1 5.0E-02 0 0
CUI: C0342686
Disease: Aromatic amino acid decarboxylase deficiency
Aromatic amino acid decarboxylase deficiency 		5 0 1 5.0E-02 0 0
CUI: C0878676
Disease: 6-pyruvoyl-tetrahydropterin synthase deficiency
6-pyruvoyl-tetrahydropterin synthase deficiency 		5 0 1 5.0E-02 0 0