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: C2936346
Disease: 22q11 Deletion Syndrome
22q11 Deletion Syndrome 		31 0 10 8.7E-02 0 0
CUI: C0431718
Disease: Multiple renal cysts
Multiple renal cysts 		46 0 11 8.5E-02 0 0
CUI: C1837731
Disease: Overfolded helix
Overfolded helix 		46 0 11 8.5E-02 0 0
CUI: C0033806
Disease: Pseudohypoparathyroidism
Pseudohypoparathyroidism 		34 0 10 8.5E-02 0 0
CUI: C2931404
Disease: Albright's hereditary osteodystrophy
Albright's hereditary osteodystrophy 		22 0 9 8.4E-02 0 0
CUI: C0030044
Disease: Acrocephaly
Acrocephaly 		35 0 10 8.4E-02 0 0
CUI: C0266383
Disease: Uterine Anomalies
Uterine Anomalies 		35 0 10 8.4E-02 0 0
CUI: C1843517
Disease: Retinal arteriolar tortuosity
Retinal arteriolar tortuosity 		23 0 9 8.3E-02 0 0
CUI: C4025838
Disease: Abnormality of the pharynx
Abnormality of the pharynx 		23 0 9 8.3E-02 0 0
CUI: C3164445
Disease: Abnormality of aortic valve
Abnormality of aortic valve 		50 0 11 8.3E-02 0 0
CUI: C1855841
Disease: Hypocalcemic seizures
Hypocalcemic seizures 		11 0 8 8.2E-02 0 0
CUI: C0036508
Disease: Seborrheic dermatitis
Seborrheic dermatitis 		39 0 10 8.1E-02 0 0
CUI: C4021797
Disease: Abnormality of the thorax
Abnormality of the thorax 		40 0 10 8.1E-02 0 0
CUI: C0020503
Disease: Hyperparathyroidism, Secondary
Hyperparathyroidism, Secondary 		68 4 12 8.0E-02 1 6.2E-02
CUI: C0034150
Disease: Purpura
Purpura 		68 0 12 8.0E-02 0 0
CUI: C4048195
Disease: Autosomal dominant hypocalcemia
Autosomal dominant hypocalcemia 		29 9 9 7.9E-02 6 0.38
CUI: C0014130
Disease: Endocrine System Diseases
Endocrine System Diseases 		74 0 12 7.7E-02 0 0
CUI: C0220704
Disease: Shprintzen syndrome
Shprintzen syndrome 		46 0 10 7.7E-02 0 0
CUI: C0685695
Disease: Abnormal lung lobation
Abnormal lung lobation 		32 0 9 7.7E-02 0 0
CUI: C0041207
Disease: Truncus Arteriosus, Persistent
Truncus Arteriosus, Persistent 		76 0 12 7.6E-02 0 0
CUI: C0685891
Disease: Congenital hypoplasia of thymus
Congenital hypoplasia of thymus 		34 0 9 7.6E-02 0 0
CUI: C0078982
Disease: Arhinencephaly
Arhinencephaly 		35 0 9 7.5E-02 0 0
CUI: C0085859
Disease: Polyglandular Type I Autoimmune Syndrome
Polyglandular Type I Autoimmune Syndrome 		64 0 11 7.5E-02 0 0
CUI: C0566620
Disease: Nasal voice
Nasal voice 		93 0 13 7.5E-02 0 0
CUI: C0231528
Disease: Myalgia
Myalgia 		226 0 22 7.4E-02 0 0