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: C0151686
Disease: Growth retardation
Growth retardation 		1 0 1 2.6E-02 0 0
CUI: C0152112
Disease: Foster-Kennedy Syndrome
Foster-Kennedy Syndrome 		1 0 1 2.6E-02 0 0
CUI: C0234259
Disease: Sensitive to smells
Sensitive to smells 		1 0 1 2.6E-02 0 0
CUI: C0238391
Disease: PRIMARY LACTIC ACIDOSIS
PRIMARY LACTIC ACIDOSIS 		1 0 1 2.6E-02 0 0
CUI: C0238637
Disease: Anal pain
Anal pain 		1 0 1 2.6E-02 0 0
CUI: C0240940
Disease: Scalp pain
Scalp pain 		1 0 1 2.6E-02 0 0
CUI: C0271291
Disease: Corneal anesthesia
Corneal anesthesia 		1 0 1 2.6E-02 0 0
CUI: C0563632
Disease: Manifest-latent nystagmus
Manifest-latent nystagmus 		1 0 1 2.6E-02 0 0
CUI: C0751402
Disease: Optic Disk Disorders
Optic Disk Disorders 		1 0 1 2.6E-02 0 0
CUI: C0795927
Disease: Deafness, congenital onychodystrophy, recessive form
Deafness, congenital onychodystrophy, recessive form 		1 0 1 2.6E-02 0 0
CUI: C1266176
Disease: Atypical choroid plexus papilloma
Atypical choroid plexus papilloma 		1 0 1 2.6E-02 0 0
CUI: C1333084
Disease: Colon Neuroendocrine Tumor G1
Colon Neuroendocrine Tumor G1 		1 0 1 2.6E-02 0 0
CUI: C1333100
Disease: Squamous cell carcinoma of colon
Squamous cell carcinoma of colon 		1 0 1 2.6E-02 0 0
CUI: C1836474
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7 		1 0 1 2.6E-02 0 0
CUI: C1842382
Disease: Epilepsy, Benign Neonatal, 3
Epilepsy, Benign Neonatal, 3 		1 0 1 2.6E-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 2.6E-02 0 0
CUI: C1843244
Disease: EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2 		1 0 1 2.6E-02 0 0
CUI: C1846722
Disease: Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies
Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies 		1 0 1 2.6E-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 2.6E-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 2.6E-02 0 0
CUI: C1860165
Disease: Pulmonary valve defects
Pulmonary valve defects 		1 0 1 2.6E-02 0 0
CUI: C1970160
Disease: Epilepsy, Childhood Absence, Susceptibility To, 4
Epilepsy, Childhood Absence, Susceptibility To, 4 		1 0 1 2.6E-02 0 0
CUI: C2315667
Disease: Fetal microcephaly
Fetal microcephaly 		1 0 1 2.6E-02 0 0
CUI: C2675185
Disease: Kahrizi Syndrome
Kahrizi Syndrome 		1 0 1 2.6E-02 0 0
CUI: C2677326
Disease: Epileptic Encephalopathy, Early Infantile, 4
Epileptic Encephalopathy, Early Infantile, 4 		1 0 1 2.6E-02 0 0