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: C1855304
Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 1
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 1 		8 0 4 0.17 0 0
CUI: C4022016
Disease: Abnormality of the preputium
Abnormality of the preputium 		22 0 6 0.17 0 0
CUI: C4023917
Disease: Aplasia/Hypoplasia of the uvula
Aplasia/Hypoplasia of the uvula 		22 0 6 0.17 0 0
CUI: C4025071
Disease: Aplasia/Hypoplasia of fingers
Aplasia/Hypoplasia of fingers 		22 0 6 0.17 0 0
CUI: C0272027
Disease: Pyridoxine-responsive sideroblastic anemia
Pyridoxine-responsive sideroblastic anemia 		24 0 6 0.16 0 0
CUI: C0342526
Disease: Absent testes
Absent testes 		24 0 6 0.16 0 0
CUI: C0238093
Disease: Stenosis of duodenum
Stenosis of duodenum 		29 0 6 0.14 0 0
CUI: C1841984
Disease: GLOMUVENOUS MALFORMATIONS
GLOMUVENOUS MALFORMATIONS 		13 0 4 0.14 0 0
CUI: C1859569
Disease: BARDET-BIEDL SYNDROME 11
BARDET-BIEDL SYNDROME 11 		5 0 3 0.14 0 0
CUI: C4025756
Disease: Abnormal aortic morphology
Abnormal aortic morphology 		29 0 6 0.14 0 0
CUI: C0151640
Disease: Decreased fertility in males
Decreased fertility in males 		30 0 6 0.14 0 0
CUI: C3887489
Disease: Clubbing of toes
Clubbing of toes 		30 0 6 0.14 0 0
CUI: C4025211
Disease: Abnormal carotid artery morphology
Abnormal carotid artery morphology 		32 0 6 0.13 0 0
CUI: C0524582
Disease: Mulibrey Nanism
Mulibrey Nanism 		7 0 3 0.13 0 0
CUI: C0795858
Disease: Chromosome 15q, trisomy
Chromosome 15q, trisomy 		7 0 3 0.13 0 0
CUI: C4021750
Disease: Abnormality of femur morphology
Abnormality of femur morphology 		33 0 6 0.13 0 0
CUI: C4551705
Disease: Abnormality of chromosome stability
Abnormality of chromosome stability 		34 0 6 0.13 0 0
CUI: C1859305
Disease: Cerebellar Ataxia and Hypogonadotropic Hypogonadism
Cerebellar Ataxia and Hypogonadotropic Hypogonadism 		8 0 3 0.12 0 0
CUI: C2608055
Disease: Hereditary Renal Cell Carcinoma
Hereditary Renal Cell Carcinoma 		8 0 3 0.12 0 0
CUI: C4021737
Disease: Chromosomal breakage induced by crosslinking agents
Chromosomal breakage induced by crosslinking agents 		8 0 3 0.12 0 0
CUI: C2749463
Disease: Aplasia/Hypoplasia of the radius
Aplasia/Hypoplasia of the radius 		45 0 7 0.12 0 0
CUI: C4020968
Disease: Abnormal localization of kidney
Abnormal localization of kidney 		40 0 6 0.11 0 0
CUI: C4024780
Disease: Almond-shaped palpebral fissure
Almond-shaped palpebral fissure 		40 0 6 0.11 0 0
CUI: C0015558
Disease: Fallopian Tube Neoplasms
Fallopian Tube Neoplasms 		2 0 2 0.11 0 0
CUI: C0266387
Disease: Bicornuate uterus
Bicornuate uterus 		44 0 6 0.11 0 0