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: C0795910
Disease: COWCHOCK SYNDROME
COWCHOCK SYNDROME 		3 0 3 0.75 0 0
CUI: C4225180
Disease: EVEN-PLUS SYNDROME
EVEN-PLUS SYNDROME 		2 0 2 0.50 0 0
CUI: C1845095
Disease: DEAFNESS, X-LINKED 5 (disorder)
DEAFNESS, X-LINKED 5 (disorder) 		1 0 1 0.25 0 0
CUI: C1970840
Disease: Leukoencephalopathy With Metaphyseal Chondrodysplasia
Leukoencephalopathy With Metaphyseal Chondrodysplasia 		1 0 1 0.25 0 0
CUI: C1970887
Disease: Abnormal middle ear reflexes
Abnormal middle ear reflexes 		1 0 1 0.25 0 0
CUI: C3151753
Disease: COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6 		1 0 1 0.25 0 0
CUI: C3808414
Disease: PERRAULT SYNDROME 3
PERRAULT SYNDROME 3 		1 0 1 0.25 0 0
CUI: C4021991
Disease: Abnormality of the astrocytes
Abnormality of the astrocytes 		1 0 1 0.25 0 0
CUI: C4225428
Disease: ANEMIA, SIDEROBLASTIC, 4
ANEMIA, SIDEROBLASTIC, 4 		1 0 1 0.25 0 0
CUI: C4280736
Disease: Large knee
Large knee 		1 0 1 0.25 0 0
CUI: C4304400
Disease: X-linked hereditary sensory and autonomic neuropathy with deafness
X-linked hereditary sensory and autonomic neuropathy with deafness 		1 0 1 0.25 0 0
CUI: C0597647
Disease: viral leukemogenesis
viral leukemogenesis 		2 0 1 0.20 0 0
CUI: C1533163
Disease: Disorder of cellular component of blood
Disorder of cellular component of blood 		2 0 1 0.20 0 0
CUI: C1836752
Disease: Abnormal speech discrimination
Abnormal speech discrimination 		2 0 1 0.20 0 0
CUI: C3554105
Disease: PERRAULT SYNDROME 2
PERRAULT SYNDROME 2 		2 0 1 0.20 0 0
CUI: C3809105
Disease: PERRAULT SYNDROME 4
PERRAULT SYNDROME 4 		2 0 1 0.20 0 0
CUI: C4021862
Disease: Absent epiphyses
Absent epiphyses 		2 0 1 0.20 0 0
CUI: C4274077
Disease: Autosomal recessive sideroblastic anemia
Autosomal recessive sideroblastic anemia 		2 0 1 0.20 0 0
CUI: C4274109
Disease: Autosomal dominant Charcot-Marie-Tooth disease type 2D
Autosomal dominant Charcot-Marie-Tooth disease type 2D 		2 0 1 0.20 0 0
CUI: C4551721
Disease: PERRAULT SYNDROME 1
PERRAULT SYNDROME 1 		2 0 1 0.20 0 0
CUI: C0272214
Disease: Persistent lymphocytosis
Persistent lymphocytosis 		3 0 1 0.17 0 0
CUI: C0424693
Disease: Broad skull
Broad skull 		3 0 1 0.17 0 0
CUI: C1839413
Disease: Pyruvate Dehydrogenase E1 Alpha Deficiency
Pyruvate Dehydrogenase E1 Alpha Deficiency 		3 0 1 0.17 0 0
CUI: C4021251
Disease: Dysplasia of the femoral head
Dysplasia of the femoral head 		3 0 1 0.17 0 0
CUI: C1834954
Disease: Coronal cleft vertebrae
Coronal cleft vertebrae 		11 0 2 0.15 0 0