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: C0266677
Disease: Synotus
Synotus 		2 0 1 0.11 0 0
CUI: C0345397
Disease: Accessory rib
Accessory rib 		12 0 2 0.11 0 0
CUI: C0685628
Disease: Full supernumerary rib
Full supernumerary rib 		2 0 1 0.11 0 0
CUI: C1835895
Disease: RETINITIS PIGMENTOSA 33 (disorder)
RETINITIS PIGMENTOSA 33 (disorder) 		2 0 1 0.11 0 0
CUI: C1859774
Disease: Optic Nerve Hypoplasia and Abnormalities of the Central Nervous System
Optic Nerve Hypoplasia and Abnormalities of the Central Nervous System 		2 0 1 0.11 0 0
CUI: C2674403
Disease: Scleral thickening
Scleral thickening 		2 0 1 0.11 0 0
CUI: C3150968
Disease: MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 6
MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 6 		2 0 1 0.11 0 0
CUI: C3151380
Disease: SCHIZOPHRENIA 15
SCHIZOPHRENIA 15 		2 0 1 0.11 0 0
CUI: C4024163
Disease: Abnormal temporal bone morphology
Abnormal temporal bone morphology 		2 0 1 0.11 0 0
CUI: C4025301
Disease: Cervical C5/C6 vertebrae fusion
Cervical C5/C6 vertebrae fusion 		2 0 1 0.11 0 0
CUI: C4225424
Disease: OPTIC DISC ANOMALIES WITH RETINAL AND/OR MACULAR DYSTROPHY
OPTIC DISC ANOMALIES WITH RETINAL AND/OR MACULAR DYSTROPHY 		2 0 1 0.11 0 0
CUI: C1844752
Disease: Butterfly vertebrae
Butterfly vertebrae 		13 0 2 0.11 0 0
CUI: C1843496
Disease: Bilateral microphthalmos
Bilateral microphthalmos 		35 0 4 0.10 0 0
CUI: C0039981
Disease: Thoracic Neoplasms
Thoracic Neoplasms 		3 0 1 1.0E-01 0 0
CUI: C1395317
Disease: Dextrocardia with situs inversus
Dextrocardia with situs inversus 		3 0 1 1.0E-01 0 0
CUI: C1876185
Disease: Dysgnathia complex
Dysgnathia complex 		3 0 1 1.0E-01 0 0
CUI: C4274282
Disease: Nanophthalmia
Nanophthalmia 		3 0 1 1.0E-01 0 0
CUI: C0265242
Disease: Otocephaly
Otocephaly 		4 0 1 9.1E-02 0 0
CUI: C1519172
Disease: Salivary Gland Carcinoma ex Pleomorphic Adenoma
Salivary Gland Carcinoma ex Pleomorphic Adenoma 		4 0 1 9.1E-02 0 0
CUI: C1833798
Disease: Optic Nerve Aplasia, Bilateral
Optic Nerve Aplasia, Bilateral 		4 0 1 9.1E-02 0 0
CUI: C1864871
Disease: Chromosome 17q21.31 Deletion Syndrome
Chromosome 17q21.31 Deletion Syndrome 		4 0 1 9.1E-02 0 0
CUI: C1865295
Disease: Auriculo-condylar syndrome
Auriculo-condylar syndrome 		4 0 1 9.1E-02 0 0
CUI: C4020963
Disease: Absent nares
Absent nares 		4 0 1 9.1E-02 0 0
CUI: C1854510
Disease: Abnormality of the cranial nerves
Abnormality of the cranial nerves 		17 0 2 8.7E-02 0 0
CUI: C0229197
Disease: Retinal fold (finding)
Retinal fold (finding) 		5 0 1 8.3E-02 0 0