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: C1961835
Disease: Gaucher Disease, Type 1
Gaucher Disease, Type 1 		48 0 6 6.6E-02 0 0
CUI: C0020651
Disease: Hypotension, Orthostatic
Hypotension, Orthostatic 		82 0 8 6.5E-02 0 0
CUI: C0267963
Disease: Exocrine pancreatic insufficiency
Exocrine pancreatic insufficiency 		82 0 8 6.5E-02 0 0
CUI: C0026985
Disease: Myelodysplasia
Myelodysplasia 		181 0 14 6.5E-02 0 0
CUI: C0002886
Disease: Anemia, Macrocytic
Anemia, Macrocytic 		51 0 6 6.4E-02 0 0
CUI: C0426789
Disease: Short thorax
Short thorax 		51 0 6 6.4E-02 0 0
CUI: C1334011
Disease: High Grade Cervical Intraepithelial Neoplasia
High Grade Cervical Intraepithelial Neoplasia 		51 0 6 6.4E-02 0 0
CUI: C0205875
Disease: Papillomatosis
Papillomatosis 		18 0 4 6.3E-02 0 0
CUI: C0023453
Disease: L2 Acute Lymphoblastic Leukemia
L2 Acute Lymphoblastic Leukemia 		53 0 6 6.2E-02 0 0
CUI: C0038238
Disease: Steatorrhea
Steatorrhea 		37 0 5 6.2E-02 0 0
CUI: C0265290
Disease: Metaphyseal chondrodysplasia
Metaphyseal chondrodysplasia 		20 0 4 6.2E-02 0 0
CUI: C1527383
Disease: Morphea
Morphea 		20 0 4 6.2E-02 0 0
CUI: C1850083
Disease: Irregular ossification at anterior rib ends
Irregular ossification at anterior rib ends 		3 0 3 6.1E-02 0 0
CUI: C0242621
Disease: Isochromosomes
Isochromosomes 		75 0 7 6.0E-02 0 0
CUI: C0238348
Disease: Squamous cell carcinoma of penis
Squamous cell carcinoma of penis 		40 0 5 6.0E-02 0 0
CUI: C2825139
Disease: Acute Myeloid Leukemia with Myelodysplasia-Related Changes
Acute Myeloid Leukemia with Myelodysplasia-Related Changes 		23 0 4 5.9E-02 0 0
CUI: C0264490
Disease: Acute respiratory failure
Acute respiratory failure 		78 0 7 5.8E-02 0 0
CUI: C0085702
Disease: Monocytosis
Monocytosis 		61 0 6 5.8E-02 0 0
CUI: C1838702
Disease: Retinitis Pigmentosa 13
Retinitis Pigmentosa 13 		6 0 3 5.8E-02 0 0
CUI: C0334070
Disease: Maturation defect
Maturation defect 		43 0 5 5.7E-02 0 0
CUI: C1849039
Disease: Metaphyseal widening
Metaphyseal widening 		43 0 5 5.7E-02 0 0
CUI: C0234378
Disease: Static Tremor
Static Tremor 		62 0 6 5.7E-02 0 0
CUI: C1836320
Disease: Proximal femoral metaphyseal irregularity
Proximal femoral metaphyseal irregularity 		7 0 3 5.7E-02 0 0
CUI: C1850087
Disease: Narrow sacroiliac notch
Narrow sacroiliac notch 		7 0 3 5.7E-02 0 0
CUI: C3552526
Disease: Metaphyseal sclerosis
Metaphyseal sclerosis 		7 0 3 5.7E-02 0 0