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: C0277941
Disease: Blanching of skin
Blanching of skin 		1 0 1 0.11 0 0
CUI: C1264000
Disease: Sickle cell-Hemoglobin O Arab disease
Sickle cell-Hemoglobin O Arab disease 		1 0 1 0.11 0 0
CUI: C1292231
Disease: In(Lu) phenotype (finding)
In(Lu) phenotype (finding) 		1 0 1 0.11 0 0
CUI: C1857719
Disease: Anemia, Diamond-Blackfan, 3
Anemia, Diamond-Blackfan, 3 		1 0 1 0.11 0 0
CUI: C1858990
Disease: Beta Thalassemia, Dominant Inclusion Body Type
Beta Thalassemia, Dominant Inclusion Body Type 		1 0 1 0.11 0 0
CUI: C2986691
Disease: Inherited bone marrow failure syndrome
Inherited bone marrow failure syndrome 		11 0 2 0.11 0 0
CUI: C3150805
Disease: FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 6
FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 6 		1 0 1 0.11 0 0
CUI: C3151421
Disease: CYANOSIS, TRANSIENT NEONATAL
CYANOSIS, TRANSIENT NEONATAL 		1 0 1 0.11 0 0
CUI: C3161373
Disease: Dominant thalassemia
Dominant thalassemia 		1 0 1 0.11 0 0
CUI: C3274463
Disease: Sickle Beta 0 Thalassemia
Sickle Beta 0 Thalassemia 		1 0 1 0.11 0 0
CUI: C3889873
Disease: HEMOGLOBIN SAINT ETIENNE PHENOTYPE
HEMOGLOBIN SAINT ETIENNE PHENOTYPE 		1 0 1 0.11 0 0
CUI: C3889898
Disease: HEMOGLOBIN C PHENOTYPE
HEMOGLOBIN C PHENOTYPE 		1 0 1 0.11 0 0
CUI: C3891694
Disease: HEMOGLOBIN TUBINGEN PHENOTYPE
HEMOGLOBIN TUBINGEN PHENOTYPE 		1 0 1 0.11 0 0
CUI: C4016175
Disease: HEMOGLOBIN HOUSTON PHENOTYPE
HEMOGLOBIN HOUSTON PHENOTYPE 		1 0 1 0.11 0 0
CUI: C4017494
Disease: BETA-KNOSSOS-THALASSEMIA
BETA-KNOSSOS-THALASSEMIA 		1 0 1 0.11 0 0
CUI: C4017510
Disease: BETA-MALAY-THALASSEMIA
BETA-MALAY-THALASSEMIA 		1 0 1 0.11 0 0
CUI: C4017522
Disease: BETA-SHOWA-YAKUSHIJI THALASSEMIA
BETA-SHOWA-YAKUSHIJI THALASSEMIA 		1 0 1 0.11 0 0
CUI: C4017525
Disease: BETA-PLUS-THALASSEMIA, DOMINANT
BETA-PLUS-THALASSEMIA, DOMINANT 		1 0 1 0.11 0 0
CUI: C4017528
Disease: BETA-THALASSEMIA, LERMONTOV TYPE
BETA-THALASSEMIA, LERMONTOV TYPE 		1 0 1 0.11 0 0
CUI: C4023619
Disease: Absence of Lutheran antigen on erythrocytes
Absence of Lutheran antigen on erythrocytes 		1 0 1 0.11 0 0
CUI: C4024695
Disease: Increased red cell sickling tendency
Increased red cell sickling tendency 		1 0 1 0.11 0 0
CUI: C4284047
Disease: HEMOGLOBIN AUBENAS PHENOTYPE
HEMOGLOBIN AUBENAS PHENOTYPE 		1 0 1 0.11 0 0
CUI: C4284050
Disease: HEMOGLOBIN GAMBARA PHENOTYPE
HEMOGLOBIN GAMBARA PHENOTYPE 		1 0 1 0.11 0 0
CUI: C4310744
Disease: BONE MARROW FAILURE SYNDROME 3
BONE MARROW FAILURE SYNDROME 3 		1 0 1 0.11 0 0
CUI: C4310971
Disease: HB NIIGATA
HB NIIGATA 		1 0 1 0.11 0 0