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: C0021177
Disease: Increased Libido
Increased Libido 		1 0 1 1.0E-01 0 0
CUI: C0154695
Disease: Diplegic Infantile Cerebral Palsy
Diplegic Infantile Cerebral Palsy 		1 0 1 1.0E-01 0 0
CUI: C0154697
Disease: Cerebral Palsy, Quadriplegic, Infantile
Cerebral Palsy, Quadriplegic, Infantile 		1 0 1 1.0E-01 0 0
CUI: C0154698
Disease: Monoplegic Infantile Cerebral Palsy
Monoplegic Infantile Cerebral Palsy 		1 0 1 1.0E-01 0 0
CUI: C0234259
Disease: Sensitive to smells
Sensitive to smells 		1 0 1 1.0E-01 0 0
CUI: C0238637
Disease: Anal pain
Anal pain 		1 0 1 1.0E-01 0 0
CUI: C0240940
Disease: Scalp pain
Scalp pain 		1 0 1 1.0E-01 0 0
CUI: C0264725
Disease: Acute left-sided heart failure
Acute left-sided heart failure 		1 0 1 1.0E-01 0 0
CUI: C0270807
Disease: Monoplegic Cerebral Palsy
Monoplegic Cerebral Palsy 		1 0 1 1.0E-01 0 0
CUI: C0271291
Disease: Corneal anesthesia
Corneal anesthesia 		1 0 1 1.0E-01 0 0
CUI: C0393725
Disease: Eating epilepsy
Eating epilepsy 		1 0 1 1.0E-01 0 0
CUI: C0394003
Disease: Cerebral Palsy, Dystonic-Rigid
Cerebral Palsy, Dystonic-Rigid 		1 0 1 1.0E-01 0 0
CUI: C0394007
Disease: Cerebral Palsy, Atonic
Cerebral Palsy, Atonic 		1 0 1 1.0E-01 0 0
CUI: C0549471
Disease: Pancoast Tumor
Pancoast Tumor 		1 0 1 1.0E-01 0 0
CUI: C0598121
Disease: Hypoglycorrhachia
Hypoglycorrhachia 		1 0 1 1.0E-01 0 0
CUI: C0745261
Disease: Infantile apnea
Infantile apnea 		1 0 1 1.0E-01 0 0
CUI: C0751024
Disease: Cerebral Palsy, Mixed
Cerebral Palsy, Mixed 		1 0 1 1.0E-01 0 0
CUI: C0751025
Disease: Cerebral Palsy, Rolandic Type
Cerebral Palsy, Rolandic Type 		1 0 1 1.0E-01 0 0
CUI: C0751059
Disease: Cranial Neuropathies, Multiple
Cranial Neuropathies, Multiple 		1 0 1 1.0E-01 0 0
CUI: C0751141
Disease: Facial Palsy, Upper Motor Neuron
Facial Palsy, Upper Motor Neuron 		1 0 1 1.0E-01 0 0
CUI: C0751142
Disease: Facial Palsy, Lower Motor Neuron
Facial Palsy, Lower Motor Neuron 		1 0 1 1.0E-01 0 0
CUI: C0751143
Disease: Hemifacial Paralysis
Hemifacial Paralysis 		1 0 1 1.0E-01 0 0
CUI: C0795865
Disease: Chromosome 17, trisomy 17p
Chromosome 17, trisomy 17p 		1 0 1 1.0E-01 0 0
CUI: C0852698
Disease: 17,20-desmolase deficiency
17,20-desmolase deficiency 		1 0 1 1.0E-01 0 0
CUI: C0871007
Disease: snake phobia
snake phobia 		1 0 1 1.0E-01 0 0