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: C4025701
Disease: Abnormality of the cerebral cortex
Abnormality of the cerebral cortex 		11 0 1 7.7E-02 0 0
CUI: C4082197
Disease: Charcot-Marie-Tooth disease type 4
Charcot-Marie-Tooth disease type 4 		14 0 1 6.2E-02 0 0
CUI: C0302280
Disease: Adrenogenital Syndrome
Adrenogenital Syndrome 		16 0 1 5.6E-02 0 0
CUI: C3805839
Disease: Central hypoventilation
Central hypoventilation 		16 0 1 5.6E-02 0 0
CUI: C0234649
Disease: Abnormal saccadic eye movement
Abnormal saccadic eye movement 		17 0 1 5.3E-02 0 0
CUI: C1842820
Disease: Cardiac conduction abnormality
Cardiac conduction abnormality 		18 0 1 5.0E-02 0 0
CUI: C4025614
Disease: EMG: chronic denervation signs
EMG: chronic denervation signs 		18 0 1 5.0E-02 0 0
CUI: C0341306
Disease: Microvillus inclusion disease
Microvillus inclusion disease 		19 0 1 4.8E-02 0 0
CUI: C4274414
Disease: Epstein-Barr virus associated gastric carcinoma
Epstein-Barr virus associated gastric carcinoma 		20 0 1 4.5E-02 0 0
CUI: C0346040
Disease: Stage 0 Skin Melanoma
Stage 0 Skin Melanoma 		21 0 1 4.3E-02 0 0
CUI: C1838114
Disease: Generalized limb muscle atrophy
Generalized limb muscle atrophy 		21 0 1 4.3E-02 0 0
CUI: C1850601
Disease: Abnormality of brainstem morphology
Abnormality of brainstem morphology 		21 0 1 4.3E-02 0 0
CUI: C0268070
Disease: Hypocupremia
Hypocupremia 		23 0 1 4.0E-02 0 0
CUI: C1969443
Disease: Trifunctional Protein Deficiency With Myopathy And Neuropathy
Trifunctional Protein Deficiency With Myopathy And Neuropathy 		23 0 1 4.0E-02 0 0
CUI: C0264694
Disease: Chronic myocardial ischemia
Chronic myocardial ischemia 		29 0 1 3.2E-02 0 0
CUI: C4725861
Disease: Metastatic Malignant Neoplasm in the Viscera
Metastatic Malignant Neoplasm in the Viscera 		30 0 1 3.1E-02 0 0
CUI: C0038450
Disease: Stridor
Stridor 		31 7 1 3.0E-02 1 8.3E-02
CUI: C0270971
Disease: Floppy infant syndrome
Floppy infant syndrome 		31 0 1 3.0E-02 0 0
CUI: C0271683
Disease: Polyneuropathy, Motor
Polyneuropathy, Motor 		32 0 1 2.9E-02 0 0
CUI: C0043116
Disease: HMN (Hereditary Motor Neuropathy) Proximal Type I
HMN (Hereditary Motor Neuropathy) Proximal Type I 		34 0 1 2.8E-02 0 0
CUI: C4024923
Disease: Diffuse white matter abnormalities
Diffuse white matter abnormalities 		34 0 1 2.8E-02 0 0
CUI: C1850597
Disease: Leigh Syndrome Due To Mitochondrial Complex II Deficiency
Leigh Syndrome Due To Mitochondrial Complex II Deficiency 		36 0 1 2.6E-02 0 0
CUI: C1850598
Disease: Leigh Syndrome due to Mitochondrial Complex III Deficiency
Leigh Syndrome due to Mitochondrial Complex III Deficiency 		36 0 1 2.6E-02 0 0
CUI: C1850600
Disease: Leigh Syndrome due to Mitochondrial Complex V Deficiency
Leigh Syndrome due to Mitochondrial Complex V Deficiency 		36 0 1 2.6E-02 0 0
CUI: C2931891
Disease: Necrotizing encephalopathy, infantile subacute, of Leigh
Necrotizing encephalopathy, infantile subacute, of Leigh 		36 0 1 2.6E-02 0 0