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: C0278776
Disease: recurrent childhood acute myeloid leukemia
recurrent childhood acute myeloid leukemia 		1 0 1 0.25 0 0
CUI: C0553699
Disease: Heinz body observation
Heinz body observation 		6 0 2 0.25 0 0
CUI: C0796159
Disease: Mental retardation Smith Fineman Myers type
Mental retardation Smith Fineman Myers type 		1 0 1 0.25 0 0
CUI: C1334068
Disease: Hypercellular bone marrow
Hypercellular bone marrow 		1 0 1 0.25 0 0
CUI: C1839727
Disease: Mental Retardation with Spastic Paraplegia
Mental Retardation with Spastic Paraplegia 		1 0 1 0.25 0 0
CUI: C2697573
Disease: Heinz-Ehrlich Body Measurement
Heinz-Ehrlich Body Measurement 		6 0 2 0.25 0 0
CUI: C2873755
Disease: Triple gene defect alpha thalassemia
Triple gene defect alpha thalassemia 		1 0 1 0.25 0 0
CUI: C3161173
Disease: Hemoglobin H Constant Spring
Hemoglobin H Constant Spring 		1 0 1 0.25 0 0
CUI: C3161175
Disease: Hydrops fetalis due to alpha thalassemia
Hydrops fetalis due to alpha thalassemia 		1 0 1 0.25 0 0
CUI: C4016148
Disease: ALPHA-THALASSEMIA-2, NONDELETIONAL
ALPHA-THALASSEMIA-2, NONDELETIONAL 		1 0 1 0.25 0 0
CUI: C4016158
Disease: ALPHA-THALASSEMIA, HMONG TYPE
ALPHA-THALASSEMIA, HMONG TYPE 		1 0 1 0.25 0 0
CUI: C4016452
Disease: MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED
MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED 		1 0 1 0.25 0 0
CUI: C4021070
Disease: Absent mastoid
Absent mastoid 		1 0 1 0.25 0 0
CUI: C4021166
Disease: Bridged palmar crease
Bridged palmar crease 		1 0 1 0.25 0 0
CUI: C4021839
Disease: Abnormal dense granule content
Abnormal dense granule content 		1 0 1 0.25 0 0
CUI: C4022543
Disease: Accessory scrotum
Accessory scrotum 		1 0 1 0.25 0 0
CUI: C4022863
Disease: Abnormal alpha granule content
Abnormal alpha granule content 		1 0 1 0.25 0 0
CUI: C4023950
Disease: Enlarged epiphyses of the distal phalanges of the hand
Enlarged epiphyses of the distal phalanges of the hand 		1 0 1 0.25 0 0
CUI: C4284348
Disease: HEMOGLOBIN EVANSTON PHENOTYPE
HEMOGLOBIN EVANSTON PHENOTYPE 		1 0 1 0.25 0 0
CUI: C0221019
Disease: Sickle cell-beta-thalassemia
Sickle cell-beta-thalassemia 		7 0 2 0.22 0 0
CUI: C0271990
Disease: delta-Thalassemia
delta-Thalassemia 		7 0 2 0.22 0 0
CUI: C3665425
Disease: Hemoglobin M Disease
Hemoglobin M Disease 		7 0 2 0.22 0 0
CUI: C0154733
Disease: Multiple cranial nerve palsy
Multiple cranial nerve palsy 		2 0 1 0.20 0 0
CUI: C0238159
Disease: Hemoglobin E disease
Hemoglobin E disease 		8 0 2 0.20 0 0
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous 		8 0 2 0.20 0 0