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: C1844831
Disease: Cleft Palate with Ankyloglossia
Cleft Palate with Ankyloglossia 		4 0 3 7.7E-02 0 0
CUI: C0152415
Disease: Ankyloglossia
Ankyloglossia 		19 0 4 7.5E-02 0 0
CUI: C0013911
Disease: Emaciation
Emaciation 		6 0 3 7.3E-02 0 0
CUI: C1844830
Disease: CLEFT PALATE, X-LINKED
CLEFT PALATE, X-LINKED 		9 0 3 6.8E-02 0 0
CUI: C0342790
Disease: Carnitine palmitoyl transferase 2 deficiency
Carnitine palmitoyl transferase 2 deficiency 		11 0 3 6.5E-02 0 0
CUI: C1849452
Disease: SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 2 (disorder)
SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 2 (disorder) 		11 0 3 6.5E-02 0 0
CUI: C0028432
Disease: Nose Diseases
Nose Diseases 		14 0 3 6.1E-02 0 0
CUI: C0017205
Disease: Gaucher Disease
Gaucher Disease 		143 0 10 5.8E-02 0 0
CUI: C0009766
Disease: Allergic Conjunctivitis
Allergic Conjunctivitis 		38 0 4 5.6E-02 0 0
CUI: C3829122
Disease: Mesenchymal Glioblastoma
Mesenchymal Glioblastoma 		21 0 3 5.4E-02 0 0
CUI: C0432562
Disease: Malignant lymphoma of spleen
Malignant lymphoma of spleen 		2 0 2 5.3E-02 0 0
CUI: C1394494
Disease: Cystocele (female)
Cystocele (female) 		2 0 2 5.3E-02 0 0
CUI: C1969443
Disease: Trifunctional Protein Deficiency With Myopathy And Neuropathy
Trifunctional Protein Deficiency With Myopathy And Neuropathy 		23 0 3 5.2E-02 0 0
CUI: C2825139
Disease: Acute Myeloid Leukemia with Myelodysplasia-Related Changes
Acute Myeloid Leukemia with Myelodysplasia-Related Changes 		23 0 3 5.2E-02 0 0
CUI: C0521515
Disease: Calcific tendinitis
Calcific tendinitis 		3 0 2 5.1E-02 0 0
CUI: C0751394
Disease: Cancer of Nose
Cancer of Nose 		3 0 2 5.1E-02 0 0
CUI: C4284040
Disease: FIGO Stage III Ovarian Cancer
FIGO Stage III Ovarian Cancer 		3 0 2 5.1E-02 0 0
CUI: C0278802
Disease: Recurrent Endometrial Cancer
Recurrent Endometrial Cancer 		24 0 3 5.1E-02 0 0
CUI: C0010695
Disease: Cystocele
Cystocele 		4 0 2 5.0E-02 0 0
CUI: C0265374
Disease: Warfarin syndrome
Warfarin syndrome 		4 0 2 5.0E-02 0 0
CUI: C1446783
Disease: rings tracheal
rings tracheal 		4 0 2 5.0E-02 0 0
CUI: C1829703
Disease: Carnitine palmitoyl transferase 1A deficiency
Carnitine palmitoyl transferase 1A deficiency 		4 0 2 5.0E-02 0 0
CUI: C4531094
Disease: Abnormal mitral valve physiology
Abnormal mitral valve physiology 		4 0 2 5.0E-02 0 0
CUI: C4703464
Disease: Abnormal aortic valve physiology
Abnormal aortic valve physiology 		4 0 2 5.0E-02 0 0
CUI: C0277355
Disease: Flea Infestation
Flea Infestation 		5 0 2 4.9E-02 0 0