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: C0524582
Disease: Mulibrey Nanism
Mulibrey Nanism 		7 0 3 0.33 0 0
CUI: C0795858
Disease: Chromosome 15q, trisomy
Chromosome 15q, trisomy 		7 0 3 0.33 0 0
CUI: C1859305
Disease: Cerebellar Ataxia and Hypogonadotropic Hypogonadism
Cerebellar Ataxia and Hypogonadotropic Hypogonadism 		8 0 3 0.30 0 0
CUI: C2608055
Disease: Hereditary Renal Cell Carcinoma
Hereditary Renal Cell Carcinoma 		8 0 3 0.30 0 0
CUI: C0270968
Disease: Limb-girdle muscular dystrophy type 2H
Limb-girdle muscular dystrophy type 2H 		6 0 2 0.22 0 0
CUI: C1720416
Disease: Episodic ataxia type 2 (disorder)
Episodic ataxia type 2 (disorder) 		13 0 3 0.20 0 0
CUI: C1801950
Disease: Opitz-G syndrome, type 2
Opitz-G syndrome, type 2 		13 0 3 0.20 0 0
CUI: C1841984
Disease: GLOMUVENOUS MALFORMATIONS
GLOMUVENOUS MALFORMATIONS 		13 0 3 0.20 0 0
CUI: C1843632
Disease: LEPROSY, SUSCEPTIBILITY TO, 2
LEPROSY, SUSCEPTIBILITY TO, 2 		1 0 1 0.20 0 0
CUI: C4281802
Disease: Spongiform encephalopathy
Spongiform encephalopathy 		14 0 3 0.19 0 0
CUI: C1456687
Disease: Polio and Post-Polio Syndrome
Polio and Post-Polio Syndrome 		16 0 3 0.17 0 0
CUI: C4749274
Disease: Chuvash erythrocytosis
Chuvash erythrocytosis 		17 0 3 0.16 0 0
CUI: C0221043
Disease: Liddle Syndrome
Liddle Syndrome 		19 0 3 0.14 0 0
CUI: C0523760
Disease: Lysine measurement
Lysine measurement 		3 0 1 0.14 0 0
CUI: C3160738
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP D2
FANCONI ANEMIA, COMPLEMENTATION GROUP D2 		19 0 3 0.14 0 0
CUI: C0265259
Disease: Popliteal pterygium syndrome
Popliteal pterygium syndrome 		20 0 3 0.14 0 0
CUI: C0030528
Disease: Paratyphoid Fever
Paratyphoid Fever 		4 0 1 0.12 0 0
CUI: C0043154
Disease: Dental White Spot
Dental White Spot 		22 0 3 0.12 0 0
CUI: C0240679
Disease: Pelvic girdle muscle atrophy
Pelvic girdle muscle atrophy 		4 0 1 0.12 0 0
CUI: C1853445
Disease: PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET
PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET 		4 0 1 0.12 0 0
CUI: C4288936
Disease: Hyperkalemic Mineralocorticoid Resistance
Hyperkalemic Mineralocorticoid Resistance 		22 0 3 0.12 0 0
CUI: C0340434
Disease: Dystrophic cardiomyopathy
Dystrophic cardiomyopathy 		5 0 1 0.11 0 0
CUI: C1858593
Disease: Limb-girdle muscular dystrophy, type 2E
Limb-girdle muscular dystrophy, type 2E 		5 0 1 0.11 0 0
CUI: C1449844
Disease: Pseudohypoaldosteronism, Type II
Pseudohypoaldosteronism, Type II 		27 0 3 0.10 0 0
CUI: C1740827
Disease: CLL progression
CLL progression 		28 0 3 1.0E-01 0 0