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: C1847868
Disease: Generalized aminoaciduria
Generalized aminoaciduria 		11 0 3 6.8E-02 0 0
CUI: C0369183
Disease: Erythrocyte Mean Corpuscular Hemoglobin Test
Erythrocyte Mean Corpuscular Hemoglobin Test 		13 0 3 6.5E-02 0 0
CUI: C1969144
Disease: Renal cortical cysts
Renal cortical cysts 		14 0 3 6.4E-02 0 0
CUI: C0857379
Disease: Abnormality of the pinna
Abnormality of the pinna 		85 0 7 6.1E-02 0 0
CUI: C0020617
Disease: Hypoglycemic coma
Hypoglycemic coma 		19 0 3 5.8E-02 0 0
CUI: C0265265
Disease: Aase syndrome
Aase syndrome 		2 0 2 5.6E-02 0 0
CUI: C1542667
Disease: Congenital erythroid hypoplasia
Congenital erythroid hypoplasia 		3 0 2 5.4E-02 0 0
CUI: C4023424
Disease: Prominent digit pad
Prominent digit pad 		4 3 2 5.3E-02 1 0.17
CUI: C0410916
Disease: Neonatal Death
Neonatal Death 		27 0 3 5.0E-02 0 0
CUI: C3553517
Disease: CORNELIA DE LANGE SYNDROME 4
CORNELIA DE LANGE SYNDROME 4 		6 11 2 5.0E-02 1 7.1E-02
CUI: C0001122
Disease: Acidosis
Acidosis 		28 0 3 4.9E-02 0 0
CUI: C0575897
Disease: Thumb deformity
Thumb deformity 		8 0 2 4.8E-02 0 0
CUI: C0239941
Disease: Persistence of hemoglobin F
Persistence of hemoglobin F 		9 0 2 4.7E-02 0 0
CUI: C1860789
Disease: Leukemia, Megakaryoblastic, of Down Syndrome
Leukemia, Megakaryoblastic, of Down Syndrome 		9 0 2 4.7E-02 0 0
CUI: C0678199
Disease: Anemia of inadequate production
Anemia of inadequate production 		10 0 2 4.5E-02 0 0
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		512 0 23 4.4E-02 0 0
CUI: C0685381
Disease: Congenital hypoplasia of radius
Congenital hypoplasia of radius 		37 0 3 4.3E-02 0 0
CUI: C1839603
Disease: Proximal tubulopathy
Proximal tubulopathy 		37 0 3 4.3E-02 0 0
CUI: C1844752
Disease: Butterfly vertebrae
Butterfly vertebrae 		13 0 2 4.3E-02 0 0
CUI: C0268596
Disease: Multiple Acyl Coenzyme A Dehydrogenase Deficiency
Multiple Acyl Coenzyme A Dehydrogenase Deficiency 		39 0 3 4.2E-02 0 0
CUI: C1864997
Disease: Majeed syndrome
Majeed syndrome 		15 0 2 4.1E-02 0 0
CUI: C1969653
Disease: MUNGAN SYNDROME
MUNGAN SYNDROME 		15 0 2 4.1E-02 0 0
CUI: C0268238
Disease: Triglyceride storage disease with ichthyosis
Triglyceride storage disease with ichthyosis 		41 0 3 4.1E-02 0 0
CUI: C0270496
Disease: Schizoaffective disorder, bipolar type
Schizoaffective disorder, bipolar type 		17 0 2 3.9E-02 0 0
CUI: C1866190
Disease: Atresia of the external auditory canal
Atresia of the external auditory canal 		44 0 3 3.9E-02 0 0