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: C0006915
Disease: Caplan Syndrome
Caplan Syndrome 		1 0 1 0.33 0 0
CUI: C0024588
Disease: Malignant essential hypertension
Malignant essential hypertension 		1 0 1 0.33 0 0
CUI: C0271198
Disease: Scotoma, Arcuate
Scotoma, Arcuate 		1 0 1 0.33 0 0
CUI: C0339402
Disease: Birdshot chorioretinitis
Birdshot chorioretinitis 		1 0 1 0.33 0 0
CUI: C0342844
Disease: Disorder of glycoprotein metabolism
Disorder of glycoprotein metabolism 		1 0 1 0.33 0 0
CUI: C0553577
Disease: Post-tuberculous reactive arthritis
Post-tuberculous reactive arthritis 		1 0 1 0.33 0 0
CUI: C0856835
Disease: Seronegative juvenile chronic arthritis
Seronegative juvenile chronic arthritis 		1 0 1 0.33 0 0
CUI: C3277286
Disease: HYPERSENSITIVITY SYNDROME, CARBAMAZEPINE-INDUCED, SUSCEPTIBILITY TO
HYPERSENSITIVITY SYNDROME, CARBAMAZEPINE-INDUCED, SUSCEPTIBILITY TO 		1 0 1 0.33 0 0
CUI: C3536738
Disease: Lumbar meningomyelocele
Lumbar meningomyelocele 		1 0 1 0.33 0 0
CUI: C4021060
Disease: Hyperplastic labia majora
Hyperplastic labia majora 		1 0 1 0.33 0 0
CUI: C4022872
Disease: Reduced thyroxin-binding globulin
Reduced thyroxin-binding globulin 		1 0 1 0.33 0 0
CUI: C4073109
Disease: Blind-spot enlargment
Blind-spot enlargment 		1 0 1 0.33 0 0
CUI: C4280709
Disease: Impaired neutrophil chemotaxis
Impaired neutrophil chemotaxis 		1 0 1 0.33 0 0
CUI: C4531146
Disease: Impaired antigen-specific response
Impaired antigen-specific response 		1 0 1 0.33 0 0
CUI: C0003510
Disease: Aortitis Syndrome
Aortitis Syndrome 		2 0 1 0.25 0 0
CUI: C0014799
Disease: Erythroderma, Maculopapular
Erythroderma, Maculopapular 		2 0 1 0.25 0 0
CUI: C0030437
Disease: Parakeratosis Variegata
Parakeratosis Variegata 		2 0 1 0.25 0 0
CUI: C0438434
Disease: Scotoma, Ring
Scotoma, Ring 		2 0 1 0.25 0 0
CUI: C1333430
Disease: EBV-Related Hodgkin Lymphoma
EBV-Related Hodgkin Lymphoma 		2 0 1 0.25 0 0
CUI: C1869024
Disease: Severe cutaneous adverse reactions (SMQ)
Severe cutaneous adverse reactions (SMQ) 		2 0 1 0.25 0 0
CUI: C4015172
Disease: SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY
SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY 		2 0 1 0.25 0 0
CUI: C4310776
Disease: RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS
RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS 		2 0 1 0.25 0 0
CUI: C0014040
Disease: Encephalitis Lethargica
Encephalitis Lethargica 		3 0 1 0.20 0 0
CUI: C0202100
Disease: Insulin C-peptide measurement
Insulin C-peptide measurement 		3 0 1 0.20 0 0
CUI: C0235988
Disease: Serum iron low (finding)
Serum iron low (finding) 		3 0 1 0.20 0 0