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: C2827503
Disease: HFE-Associated Hereditary Hemochromatosis
HFE-Associated Hereditary Hemochromatosis 		10 3 2 7.1E-02 2 5.6E-02
CUI: C4072908
Disease: Induced vaginal delivery
Induced vaginal delivery 		10 0 2 7.1E-02 0 0
CUI: C0221182
Disease: Chordee
Chordee 		11 0 2 6.9E-02 0 0
CUI: C1849043
Disease: Soft, doughy skin
Soft, doughy skin 		11 0 2 6.9E-02 0 0
CUI: C0852413
Disease: Abnormal muscle tone
Abnormal muscle tone 		14 0 2 6.2E-02 0 0
CUI: C1856408
Disease: Infantile encephalopathy
Infantile encephalopathy 		14 0 2 6.2E-02 0 0
CUI: C0012715
Disease: Iron Metabolism Disorders
Iron Metabolism Disorders 		15 3 2 6.1E-02 2 5.6E-02
CUI: C1740801
Disease: Exaggerated startle response
Exaggerated startle response 		18 0 2 5.6E-02 0 0
CUI: C0079352
Disease: Congenital torticollis
Congenital torticollis 		19 0 2 5.4E-02 0 0
CUI: C0231274
Disease: Intolerant of heat
Intolerant of heat 		19 0 2 5.4E-02 0 0
CUI: C4022735
Disease: Cerebral white matter atrophy
Cerebral white matter atrophy 		20 0 2 5.3E-02 0 0
CUI: C4021758
Disease: Delayed CNS myelination
Delayed CNS myelination 		21 0 2 5.1E-02 0 0
CUI: C0266357
Disease: Persistent umbilical sinus
Persistent umbilical sinus 		1 0 1 5.0E-02 0 0
CUI: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis 		1 0 1 5.0E-02 0 0
CUI: C0268288
Disease: Mild steroid 21-hydroxylase deficiency
Mild steroid 21-hydroxylase deficiency 		1 0 1 5.0E-02 0 0
CUI: C0339675
Disease: Axial hypermetropia
Axial hypermetropia 		1 0 1 5.0E-02 0 0
CUI: C0865274
Disease: High-oxygen-affinity hemoglobin
High-oxygen-affinity hemoglobin 		1 0 1 5.0E-02 0 0
CUI: C1859995
Disease: Hyperandrogenism, Nonclassic Type, due to 21-Hydroxylase Deficiency
Hyperandrogenism, Nonclassic Type, due to 21-Hydroxylase Deficiency 		1 0 1 5.0E-02 0 0
CUI: C1859998
Disease: CARCINOMA, ADRENOCORTICAL, ANDROGEN-SECRETING
CARCINOMA, ADRENOCORTICAL, ANDROGEN-SECRETING 		1 0 1 5.0E-02 0 0
CUI: C2673517
Disease: PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO
PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO 		1 1 1 5.0E-02 1 2.9E-02
CUI: C2673518
Disease: PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO
PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO 		1 1 1 5.0E-02 1 2.9E-02
CUI: C2673520
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding) 		1 2 1 5.0E-02 1 2.8E-02
CUI: C3150862
Disease: HEMOCHROMATOSIS, JUVENILE, DIGENIC
HEMOCHROMATOSIS, JUVENILE, DIGENIC 		1 1 1 5.0E-02 1 2.9E-02
CUI: C3151153
Disease: ADENOMA, CORTISOL-PRODUCING
ADENOMA, CORTISOL-PRODUCING 		1 0 1 5.0E-02 0 0
CUI: C3266753
Disease: Severe left ventricular systolic dysfunction
Severe left ventricular systolic dysfunction 		1 0 1 5.0E-02 0 0