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: C0549629
Disease: Abnormal delivery
Abnormal delivery 		32 0 1 5.7E-04 0 0
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result 		32 0 1 5.7E-04 0 0
CUI: C1868672
Disease: NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE
NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE 		31 0 1 5.7E-04 0 0
CUI: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED 		30 0 1 5.7E-04 0 0
CUI: C1849295
Disease: Hypoplastic labia minora
Hypoplastic labia minora 		30 0 1 5.7E-04 0 0
CUI: C1855676
Disease: Aplasia/Hypoplasia of the cerebellar vermis
Aplasia/Hypoplasia of the cerebellar vermis 		30 0 1 5.7E-04 0 0
CUI: C3151867
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED 		30 0 1 5.7E-04 0 0
CUI: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL 		30 0 1 5.7E-04 0 0
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal 		29 0 1 5.7E-04 0 0
CUI: C2677328
Disease: Cerebral hypomyelination
Cerebral hypomyelination 		29 0 1 5.7E-04 0 0
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL 		29 0 1 5.7E-04 0 0
CUI: C0265215
Disease: Meckel-Gruber syndrome
Meckel-Gruber syndrome 		26 0 1 5.7E-04 0 0
CUI: C3808249
Disease: Abnormality of the optic disc
Abnormality of the optic disc 		26 0 1 5.7E-04 0 0
CUI: C1840457
Disease: Retinal pigment epithelial atrophy
Retinal pigment epithelial atrophy 		25 0 1 5.7E-04 0 0
CUI: C0423421
Disease: Atrophic macular change
Atrophic macular change 		24 0 1 5.7E-04 0 0
CUI: C0431376
Disease: Cobblestone Lissencephaly
Cobblestone Lissencephaly 		23 0 1 5.7E-04 0 0
CUI: C1610065
Disease: Urethral atresia
Urethral atresia 		23 0 1 5.7E-04 0 0
CUI: C0268747
Disease: Diffuse mesangial sclerosis (disorder)
Diffuse mesangial sclerosis (disorder) 		22 0 1 5.7E-04 0 0
CUI: C0237849
Disease: Peeling of skin
Peeling of skin 		21 0 1 5.8E-04 0 0
CUI: C1856660
Disease: Abnormality of the helix
Abnormality of the helix 		21 0 1 5.8E-04 0 0
CUI: C4021758
Disease: Delayed CNS myelination
Delayed CNS myelination 		21 0 1 5.8E-04 0 0
CUI: C0024507
Disease: Majewski Syndrome
Majewski Syndrome 		20 0 1 5.8E-04 0 0
CUI: C0079153
Disease: Hyperkeratosis, Epidermolytic
Hyperkeratosis, Epidermolytic 		20 0 1 5.8E-04 0 0
CUI: C0266231
Disease: Ectopic anus
Ectopic anus 		20 0 1 5.8E-04 0 0
CUI: C0268141
Disease: Xeroderma pigmentosum, group G
Xeroderma pigmentosum, group G 		20 0 1 5.8E-04 0 0