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: C0152207
Disease: Alternating Exotropia
Alternating Exotropia 		1 0 1 2.4E-02 0 0
CUI: C0234259
Disease: Sensitive to smells
Sensitive to smells 		1 0 1 2.4E-02 0 0
CUI: C0234461
Disease: aphasic
aphasic 		1 0 1 2.4E-02 0 0
CUI: C0238637
Disease: Anal pain
Anal pain 		1 0 1 2.4E-02 0 0
CUI: C0240940
Disease: Scalp pain
Scalp pain 		1 0 1 2.4E-02 0 0
CUI: C0271291
Disease: Corneal anesthesia
Corneal anesthesia 		1 0 1 2.4E-02 0 0
CUI: C0271616
Disease: Precocious female puberty
Precocious female puberty 		1 1 1 2.4E-02 1 1.0E-01
CUI: C0406821
Disease: Rhabdomyomatous mesenchymal hamartoma
Rhabdomyomatous mesenchymal hamartoma 		1 0 1 2.4E-02 0 0
CUI: C0454578
Disease: Receptive aphasia (finding)
Receptive aphasia (finding) 		1 0 1 2.4E-02 0 0
CUI: C0745186
Disease: hypoventilation syndrome
hypoventilation syndrome 		1 0 1 2.4E-02 0 0
CUI: C0795927
Disease: Deafness, congenital onychodystrophy, recessive form
Deafness, congenital onychodystrophy, recessive form 		1 0 1 2.4E-02 0 0
CUI: C0796089
Disease: LISSENCEPHALY SYNDROME, NORMAN-ROBERTS TYPE
LISSENCEPHALY SYNDROME, NORMAN-ROBERTS TYPE 		1 0 1 2.4E-02 0 0
CUI: C1272765
Disease: Minimal deviation adenocarcinoma of endocervical type
Minimal deviation adenocarcinoma of endocervical type 		1 0 1 2.4E-02 0 0
CUI: C1274890
Disease: Midline cervical cleft
Midline cervical cleft 		1 0 1 2.4E-02 0 0
CUI: C1302778
Disease: Congenital lymphatic malformation
Congenital lymphatic malformation 		1 0 1 2.4E-02 0 0
CUI: C1842382
Disease: Epilepsy, Benign Neonatal, 3
Epilepsy, Benign Neonatal, 3 		1 0 1 2.4E-02 0 0
CUI: C1842531
Disease: Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp
Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp 		1 0 1 2.4E-02 0 0
CUI: C1843244
Disease: EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2 		1 0 1 2.4E-02 0 0
CUI: C1845102
Disease: Hyperekplexia and Epilepsy
Hyperekplexia and Epilepsy 		1 0 1 2.4E-02 0 0
CUI: C1855033
Disease: Mitochondrial myopathy with lactic acidosis
Mitochondrial myopathy with lactic acidosis 		1 0 1 2.4E-02 0 0
CUI: C1858672
Disease: GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1 		1 0 1 2.4E-02 0 0
CUI: C1858674
Disease: GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3 		1 0 1 2.4E-02 0 0
CUI: C1970160
Disease: Epilepsy, Childhood Absence, Susceptibility To, 4
Epilepsy, Childhood Absence, Susceptibility To, 4 		1 0 1 2.4E-02 0 0
CUI: C2675191
Disease: Polymicrogyria, Bilateral Occipital
Polymicrogyria, Bilateral Occipital 		1 0 1 2.4E-02 0 0
CUI: C2675491
Disease: AMYOTROPHIC LATERAL SCLEROSIS 11
AMYOTROPHIC LATERAL SCLEROSIS 11 		1 0 1 2.4E-02 0 0