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: C4023029
Disease: Abnormal number of granulocyte precursors
Abnormal number of granulocyte precursors 		2 0 2 0.50 0 0
CUI: C4023030
Disease: Dysplastic granulopoesis
Dysplastic granulopoesis 		2 0 2 0.50 0 0
CUI: C1334688
Disease: Megaloblastic erythroid hyperplasia
Megaloblastic erythroid hyperplasia 		3 0 2 0.40 0 0
CUI: C0751246
Disease: Illusions, Visual
Illusions, Visual 		5 0 2 0.29 0 0
CUI: C0748397
Disease: Reynolds syndrome
Reynolds syndrome 		1 0 1 0.25 0 0
CUI: C1301356
Disease: Refractory cytopenia with multilineage dysplasia and ringed sideroblasts
Refractory cytopenia with multilineage dysplasia and ringed sideroblasts 		1 0 1 0.25 0 0
CUI: C1859120
Disease: Anterior rib punctate calcifications
Anterior rib punctate calcifications 		1 0 1 0.25 0 0
CUI: C1859121
Disease: Sternal punctate calcifications
Sternal punctate calcifications 		1 0 1 0.25 0 0
CUI: C1866048
Disease: Severe hydrops fetalis
Severe hydrops fetalis 		1 0 1 0.25 0 0
CUI: C3179244
Disease: Pseudo Pelger-Huet Anomaly
Pseudo Pelger-Huet Anomaly 		1 0 1 0.25 0 0
CUI: C4021245
Disease: Patchy variation in bone mineral density
Patchy variation in bone mineral density 		1 0 1 0.25 0 0
CUI: C4023019
Disease: Single lineage myelodysplasia
Single lineage myelodysplasia 		1 0 1 0.25 0 0
CUI: C4023036
Disease: Abnormal albumin level
Abnormal albumin level 		1 0 1 0.25 0 0
CUI: C4025815
Disease: Short diaphyses
Short diaphyses 		1 0 1 0.25 0 0
CUI: C4747922
Disease: PELGER-HUET ANOMALY WITH MILD SKELETAL ANOMALIES
PELGER-HUET ANOMALY WITH MILD SKELETAL ANOMALIES 		1 0 1 0.25 0 0
CUI: C0231779
Disease: Heel toe gait
Heel toe gait 		7 0 2 0.22 0 0
CUI: C4025187
Disease: Increased megakaryocyte count
Increased megakaryocyte count 		7 0 2 0.22 0 0
CUI: C0001361
Disease: Acute tonsillitis
Acute tonsillitis 		2 0 1 0.20 0 0
CUI: C0406191
Disease: Pseudofolliculitis
Pseudofolliculitis 		8 0 2 0.20 0 0
CUI: C0853655
Disease: Abnormal mean corpuscular volume
Abnormal mean corpuscular volume 		2 0 1 0.20 0 0
CUI: C1696466
Disease: Hepatic calcification
Hepatic calcification 		2 0 1 0.20 0 0
CUI: C1859158
Disease: Laryngeal calcification
Laryngeal calcification 		2 0 1 0.20 0 0
CUI: C4023021
Disease: Multiple lineage myelodysplasia
Multiple lineage myelodysplasia 		2 0 1 0.20 0 0
CUI: C4023090
Disease: Impaired neutrophil bactericidal activity
Impaired neutrophil bactericidal activity 		2 0 1 0.20 0 0
CUI: C4024661
Disease: Abnormality of the vertebral spinous processes
Abnormality of the vertebral spinous processes 		2 0 1 0.20 0 0