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: C1859567
Disease: BARDET-BIEDL SYNDROME 9
BARDET-BIEDL SYNDROME 9 		1 0 1 0.17 0 0
CUI: C0851734
Disease: Hepatic metabolic disorders
Hepatic metabolic disorders 		2 0 1 0.14 0 0
CUI: C4551775
Disease: Knobloch Syndrome, Type I
Knobloch Syndrome, Type I 		2 0 1 0.14 0 0
CUI: C0035637
Disease: Rinderpest
Rinderpest 		3 5 1 0.12 1 6.7E-02
CUI: C0332154
Disease: Received therapy or drug for
Received therapy or drug for 		3 5 1 0.12 1 6.7E-02
CUI: C0523957
Disease: Tryptophan measurement
Tryptophan measurement 		3 0 1 0.12 0 0
CUI: C2985306
Disease: Maternal Fever
Maternal Fever 		3 0 1 0.12 0 0
CUI: C4049573
Disease: Thrombotic vascular disease
Thrombotic vascular disease 		3 0 1 0.12 0 0
CUI: C0521686
Disease: Glaucomatous retinal degeneration
Glaucomatous retinal degeneration 		4 0 1 0.11 0 0
CUI: C0270780
Disease: Degenerative myelopathy
Degenerative myelopathy 		7 0 1 8.3E-02 0 0
CUI: C3887608
Disease: HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 1
HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 1 		8 0 1 7.7E-02 0 0
CUI: C0000832
Disease: Abruptio Placentae
Abruptio Placentae 		12 0 1 5.9E-02 0 0
CUI: C1142272
Disease: Neutrophilic dermatosis
Neutrophilic dermatosis 		12 0 1 5.9E-02 0 0
CUI: C0152439
Disease: Retinoschisis
Retinoschisis 		13 0 1 5.6E-02 0 0
CUI: C1266166
Disease: Intracortical osteosarcoma
Intracortical osteosarcoma 		13 0 1 5.6E-02 0 0
CUI: C0796085
Disease: Nance-Horan syndrome
Nance-Horan syndrome 		14 0 1 5.3E-02 0 0
CUI: C2931150
Disease: Synostotic Anterior Plagiocephaly
Synostotic Anterior Plagiocephaly 		16 0 1 4.8E-02 0 0
CUI: C0410179
Disease: Ullrich congenital muscular dystrophy 1
Ullrich congenital muscular dystrophy 1 		17 0 1 4.5E-02 0 0
CUI: C0694571
Disease: extranodal lymphoma
extranodal lymphoma 		17 0 1 4.5E-02 0 0
CUI: C0948908
Disease: Nephrotoxic serum nephritis
Nephrotoxic serum nephritis 		17 0 1 4.5E-02 0 0
CUI: C1834674
Disease: BETHLEM MYOPATHY 1
BETHLEM MYOPATHY 1 		17 0 1 4.5E-02 0 0
CUI: C3887873
Disease: Hearing Loss
Hearing Loss 		18 61 1 4.3E-02 1 1.4E-02
CUI: C4551902
Disease: Craniosynostosis, Type 1
Craniosynostosis, Type 1 		18 0 1 4.3E-02 0 0
CUI: C0027441
Disease: Nasopharyngitis
Nasopharyngitis 		19 0 1 4.2E-02 0 0
CUI: C0221239
Disease: Rapidly progressive glomerulonephritis
Rapidly progressive glomerulonephritis 		19 0 1 4.2E-02 0 0