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: C0029307
Disease: Oroya Fever
Oroya Fever 		1 0 1 3.7E-02 0 0
CUI: C0234259
Disease: Sensitive to smells
Sensitive to smells 		1 0 1 3.7E-02 0 0
CUI: C0238637
Disease: Anal pain
Anal pain 		1 0 1 3.7E-02 0 0
CUI: C0240940
Disease: Scalp pain
Scalp pain 		1 0 1 3.7E-02 0 0
CUI: C0241424
Disease: Tongue biting
Tongue biting 		1 0 1 3.7E-02 0 0
CUI: C0265113
Disease: Progressing stroke
Progressing stroke 		1 0 1 3.7E-02 0 0
CUI: C0268375
Disease: Autosomal dominant epidermolysis bullosa simplex
Autosomal dominant epidermolysis bullosa simplex 		1 0 1 3.7E-02 0 0
CUI: C0271291
Disease: Corneal anesthesia
Corneal anesthesia 		1 0 1 3.7E-02 0 0
CUI: C0275584
Disease: Cutaneous nocardiosis
Cutaneous nocardiosis 		1 0 1 3.7E-02 0 0
CUI: C0342483
Disease: Hyperreninemic hypoaldosteronism
Hyperreninemic hypoaldosteronism 		1 0 1 3.7E-02 0 0
CUI: C0343111
Disease: Naegeli syndrome
Naegeli syndrome 		1 0 1 3.7E-02 0 0
CUI: C0393693
Disease: Benign Neonatal Epilepsy, Nonfamilial
Benign Neonatal Epilepsy, Nonfamilial 		1 0 1 3.7E-02 0 0
CUI: C0477633
Disease: Cervical disc disorder
Cervical disc disorder 		1 0 1 3.7E-02 0 0
CUI: C0558489
Disease: Renal pain
Renal pain 		1 0 1 3.7E-02 0 0
CUI: C0559523
Disease: Genital tuberculosis
Genital tuberculosis 		1 0 1 3.7E-02 0 0
CUI: C0751750
Disease: Argininosuccinic Acid Synthetase Deficiency Disease, Partial
Argininosuccinic Acid Synthetase Deficiency Disease, Partial 		1 0 1 3.7E-02 0 0
CUI: C0751751
Disease: Argininosuccinic Acid Synthetase Deficiency, Complete
Argininosuccinic Acid Synthetase Deficiency, Complete 		1 0 1 3.7E-02 0 0
CUI: C1290145
Disease: Disorder of cervical spine
Disorder of cervical spine 		1 0 1 3.7E-02 0 0
CUI: C1318562
Disease: Infantile digital fibromatosis
Infantile digital fibromatosis 		1 0 1 3.7E-02 0 0
CUI: C1835888
Disease: Diarrhea 4, Malabsorptive, Congenital
Diarrhea 4, Malabsorptive, Congenital 		1 0 1 3.7E-02 0 0
CUI: C1836890
Disease: Hypoplasia of the ciliary body
Hypoplasia of the ciliary body 		1 0 1 3.7E-02 0 0
CUI: C1840365
Disease: King Denborough syndrome
King Denborough syndrome 		1 0 1 3.7E-02 0 0
CUI: C1842197
Disease: Charcot-Marie-Tooth Disease, Recessive Intermediate A
Charcot-Marie-Tooth Disease, Recessive Intermediate A 		1 0 1 3.7E-02 0 0
CUI: C1842984
Disease: Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2k
Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2k 		1 0 1 3.7E-02 0 0
CUI: C1843116
Disease: Bile acid synthesis defect, congenital, 1
Bile acid synthesis defect, congenital, 1 		1 0 1 3.7E-02 0 0