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: C0393851
Disease: Polyneuropathy, Critical Illness
Polyneuropathy, Critical Illness 		3 0 3 1.00 0 0
CUI: C0751448
Disease: Polyneuropathy, Familial
Polyneuropathy, Familial 		5 0 3 0.60 0 0
CUI: C0023138
Disease: Laurence-Moon Syndrome
Laurence-Moon Syndrome 		1 0 1 0.33 0 0
CUI: C0036219
Disease: Sarcoma, Jensen
Sarcoma, Jensen 		1 0 1 0.33 0 0
CUI: C0037050
Disease: Sick Building Syndrome
Sick Building Syndrome 		1 0 1 0.33 0 0
CUI: C0271932
Disease: Anemia of chronic renal failure
Anemia of chronic renal failure 		1 0 1 0.33 0 0
CUI: C0472713
Disease: Anemia of renal disease
Anemia of renal disease 		1 0 1 0.33 0 0
CUI: C0543645
Disease: Heterozygous hemoglobinopathy
Heterozygous hemoglobinopathy 		1 0 1 0.33 0 0
CUI: C0578736
Disease: Inguinal lymphadenopathy
Inguinal lymphadenopathy 		1 0 1 0.33 0 0
CUI: C0948437
Disease: Bone marrow dysplasia
Bone marrow dysplasia 		1 0 1 0.33 0 0
CUI: C1168215
Disease: Uremic anemia
Uremic anemia 		1 0 1 0.33 0 0
CUI: C1260334
Disease: Erythropoietin-resistant anemia
Erythropoietin-resistant anemia 		1 0 1 0.33 0 0
CUI: C1264016
Disease: Familial polycythemia vera
Familial polycythemia vera 		1 0 1 0.33 0 0
CUI: C1285373
Disease: Neonatal respiratory system disorder
Neonatal respiratory system disorder 		1 0 1 0.33 0 0
CUI: C1561829
Disease: Anemia in end stage renal disease
Anemia in end stage renal disease 		1 0 1 0.33 0 0
CUI: C1859093
Disease: Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism
Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism 		1 0 1 0.33 0 0
CUI: C1868945
Disease: Polyglobulia
Polyglobulia 		1 0 1 0.33 0 0
CUI: C2675471
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 2 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 2 (finding) 		1 0 1 0.33 0 0
CUI: C2677586
Disease: Spastic Paraplegia 39, Autosomal Recessive
Spastic Paraplegia 39, Autosomal Recessive 		1 0 1 0.33 0 0
CUI: C3150990
Disease: LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY
LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY 		1 0 1 0.33 0 0
CUI: C4025707
Disease: Abnormal motor neuron morphology
Abnormal motor neuron morphology 		1 0 1 0.33 0 0
CUI: C4693552
Disease: ERYTHROCYTOSIS, FAMILIAL, 5
ERYTHROCYTOSIS, FAMILIAL, 5 		1 0 1 0.33 0 0
CUI: C4693556
Disease: DIAMOND-BLACKFAN ANEMIA-LIKE
DIAMOND-BLACKFAN ANEMIA-LIKE 		1 0 1 0.33 0 0
CUI: C0036214
Disease: Sarcoma, Engelbreth-Holm-Swarm
Sarcoma, Engelbreth-Holm-Swarm 		2 0 1 0.25 0 0
CUI: C0271899
Disease: Normocytic normochromic anemia
Normocytic normochromic anemia 		2 0 1 0.25 0 0