Source: BEFREE ×
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: C0391970
Disease: Carcinoid tumor, malignant
Carcinoid tumor, malignant 		0 2 0 0 2 0.33
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 1 2.1E-03 0 0
CUI: C0270921
Disease: Axonal neuropathy
Axonal neuropathy 		59 0 1 2.2E-03 0 0
CUI: C0023015
Disease: Language Disorders
Language Disorders 		56 0 1 2.2E-03 0 0
CUI: C0266470
Disease: Cerebellar Hypoplasia
Cerebellar Hypoplasia 		56 0 1 2.2E-03 0 0
CUI: C0085159
Disease: Seasonal Affective Disorder
Seasonal Affective Disorder 		55 0 1 2.2E-03 0 0
CUI: C0344482
Disease: Hypoplasia of corpus callosum
Hypoplasia of corpus callosum 		55 0 1 2.2E-03 0 0
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder) 		53 0 1 2.2E-03 0 0
CUI: C0038379
Disease: Strabismus
Strabismus 		51 0 1 2.2E-03 0 0
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy 		51 0 1 2.2E-03 0 0
CUI: C0751882
Disease: Myasthenic Syndromes, Congenital
Myasthenic Syndromes, Congenital 		50 0 1 2.3E-03 0 0
CUI: C0004245
Disease: Atrioventricular Block
Atrioventricular Block 		42 0 1 2.3E-03 0 0
CUI: C0020725
Disease: Type II Mucolipidosis
Type II Mucolipidosis 		42 0 1 2.3E-03 0 0
CUI: C3179455
Disease: Niemann-Pick Disease, Type C1
Niemann-Pick Disease, Type C1 		42 0 1 2.3E-03 0 0
CUI: C0007965
Disease: Chediak-Higashi Syndrome
Chediak-Higashi Syndrome 		41 0 1 2.3E-03 0 0
CUI: C0038273
Disease: Stereotypic Movement Disorder
Stereotypic Movement Disorder 		40 0 1 2.3E-03 0 0
CUI: C0265202
Disease: Seckel syndrome
Seckel syndrome 		40 0 1 2.3E-03 0 0
CUI: C0270914
Disease: Hereditary Motor and Sensory-Neuropathy Type II
Hereditary Motor and Sensory-Neuropathy Type II 		40 0 1 2.3E-03 0 0
CUI: C0002020
Disease: Alexithymia
Alexithymia 		39 0 1 2.3E-03 0 0
CUI: C0024591
Disease: Malignant hyperpyrexia due to anesthesia
Malignant hyperpyrexia due to anesthesia 		39 0 1 2.3E-03 0 0
CUI: C0001916
Disease: Albinism
Albinism 		38 0 1 2.3E-03 0 0
CUI: C0158981
Disease: Neonatal diabetes mellitus
Neonatal diabetes mellitus 		38 0 1 2.3E-03 0 0
CUI: C0751778
Disease: Myoclonic Epilepsies, Progressive
Myoclonic Epilepsies, Progressive 		38 0 1 2.3E-03 0 0
CUI: C0856975
Disease: Autistic behavior
Autistic behavior 		38 0 1 2.3E-03 0 0
CUI: C1832097
Disease: EPIDERMAL DIFFERENTIATION COMPLEX
EPIDERMAL DIFFERENTIATION COMPLEX 		38 0 1 2.3E-03 0 0