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: C1441613
Disease: Immune diffusion
Immune diffusion 		3 0 2 9.5E-02 0 0
CUI: C1846357
Disease: Meckel syndrome type 3
Meckel syndrome type 3 		3 39 2 9.5E-02 1 9.7E-03
CUI: C1859564
Disease: Bardet-Biedl syndrome 3
Bardet-Biedl syndrome 3 		3 0 2 9.5E-02 0 0
CUI: C3808410
Disease: Gastrointestinal malrotation
Gastrointestinal malrotation 		3 2 2 9.5E-02 1 1.5E-02
CUI: C0158734
Disease: Polydactyly of toes
Polydactyly of toes 		61 0 7 9.5E-02 0 0
CUI: C0266361
Disease: True Hermaphroditism (disorder)
True Hermaphroditism (disorder) 		27 0 4 9.3E-02 0 0
CUI: C1854113
Disease: Prominent nasal bridge
Prominent nasal bridge 		180 0 17 9.3E-02 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 0 15 9.2E-02 0 0
CUI: C0221352
Disease: Syndactyly of fingers
Syndactyly of fingers 		171 0 16 9.1E-02 0 0
CUI: C1321884
Disease: Atresia of vagina
Atresia of vagina 		16 0 3 9.1E-02 0 0
CUI: C4021756
Disease: Thickened superior cerebellar peduncle
Thickened superior cerebellar peduncle 		4 0 2 9.1E-02 0 0
CUI: C3714506
Disease: Meckel syndrome type 1
Meckel syndrome type 1 		53 0 6 9.0E-02 0 0
CUI: C0152427
Disease: Polydactyly
Polydactyly 		188 43 17 8.9E-02 1 9.3E-03
CUI: C1408258
Disease: Kidney damage
Kidney damage 		5 0 2 8.7E-02 0 0
CUI: C4022906
Disease: Delayed social development
Delayed social development 		5 1 2 8.7E-02 1 1.5E-02
CUI: C0398791
Disease: Nijmegen Breakage Syndrome
Nijmegen Breakage Syndrome 		94 0 9 8.6E-02 0 0
CUI: C0037822
Disease: Speech Disorders
Speech Disorders 		183 0 16 8.6E-02 0 0
CUI: C3806218
Disease: Episodic tachypnea
Episodic tachypnea 		31 0 4 8.5E-02 0 0
CUI: C4021606
Disease: Mesoaxial hand polydactyly
Mesoaxial hand polydactyly 		6 2 2 8.3E-02 1 1.5E-02
CUI: C0221365
Disease: Double ureter
Double ureter 		34 0 4 8.0E-02 0 0
CUI: C1865060
Disease: Molar tooth sign on MRI
Molar tooth sign on MRI 		35 0 4 7.8E-02 0 0
CUI: C1395852
Disease: Polydactyly preaxial type 1
Polydactyly preaxial type 1 		49 0 5 7.8E-02 0 0
CUI: C0040412
Disease: Fissured tongue
Fissured tongue 		36 0 4 7.7E-02 0 0
CUI: C4021818
Disease: Abnormality of the ovary
Abnormality of the ovary 		8 0 2 7.7E-02 0 0
CUI: C4025844
Disease: Abnormal chorioretinal morphology
Abnormal chorioretinal morphology 		36 0 4 7.7E-02 0 0