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 2 0.67 0 0
CUI: C1838180
Disease: CODAS syndrome
CODAS syndrome 		4 0 2 0.50 0 0
CUI: C1845095
Disease: DEAFNESS, X-LINKED 5 (disorder)
DEAFNESS, X-LINKED 5 (disorder) 		1 0 1 0.50 0 0
CUI: C1970840
Disease: Leukoencephalopathy With Metaphyseal Chondrodysplasia
Leukoencephalopathy With Metaphyseal Chondrodysplasia 		1 0 1 0.50 0 0
CUI: C1970887
Disease: Abnormal middle ear reflexes
Abnormal middle ear reflexes 		1 0 1 0.50 0 0
CUI: C3151753
Disease: COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6 		1 0 1 0.50 0 0
CUI: C4021991
Disease: Abnormality of the astrocytes
Abnormality of the astrocytes 		1 0 1 0.50 0 0
CUI: C4225428
Disease: ANEMIA, SIDEROBLASTIC, 4
ANEMIA, SIDEROBLASTIC, 4 		1 0 1 0.50 0 0
CUI: C4280736
Disease: Large knee
Large knee 		1 0 1 0.50 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 0.50 0 0
CUI: C1533163
Disease: Disorder of cellular component of blood
Disorder of cellular component of blood 		2 0 1 0.33 0 0
CUI: C1836752
Disease: Abnormal speech discrimination
Abnormal speech discrimination 		2 0 1 0.33 0 0
CUI: C4274077
Disease: Autosomal recessive sideroblastic anemia
Autosomal recessive sideroblastic anemia 		2 0 1 0.33 0 0
CUI: C4274109
Disease: Autosomal dominant Charcot-Marie-Tooth disease type 2D
Autosomal dominant Charcot-Marie-Tooth disease type 2D 		2 0 1 0.33 0 0
CUI: C4021251
Disease: Dysplasia of the femoral head
Dysplasia of the femoral head 		3 0 1 0.25 0 0
CUI: C4523967
Disease: Fracture infection
Fracture infection 		4 0 1 0.20 0 0
CUI: C0156409
Disease: Postmenopausal atrophic vaginitis
Postmenopausal atrophic vaginitis 		5 0 1 0.17 0 0
CUI: C0221392
Disease: Atrophic Vaginitis
Atrophic Vaginitis 		5 0 1 0.17 0 0
CUI: C4022749
Disease: Abnormal brainstem MRI signal intensity
Abnormal brainstem MRI signal intensity 		5 0 1 0.17 0 0
CUI: C4023607
Disease: Abnormal corpus striatum morphology
Abnormal corpus striatum morphology 		5 0 1 0.17 0 0
CUI: C1262037
Disease: Diabetic cystopathy
Diabetic cystopathy 		6 0 1 0.14 0 0
CUI: C1313952
Disease: Respiration intermittent
Respiration intermittent 		6 0 1 0.14 0 0
CUI: C4551551
Disease: X-linked hereditary motor and sensory neuropathy
X-linked hereditary motor and sensory neuropathy 		7 0 1 0.12 0 0
CUI: C1838663
Disease: Enlargement of the wrists
Enlargement of the wrists 		8 0 1 0.11 0 0
CUI: C3203533
Disease: Psychological Trauma
Psychological Trauma 		8 0 1 0.11 0 0