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: C0039621
Disease: Tetany
Tetany 		24 0 9 0.11 0 0
CUI: C0158733
Disease: Hand polydactyly
Hand polydactyly 		75 0 14 0.11 0 0
CUI: C0030044
Disease: Acrocephaly
Acrocephaly 		35 0 10 0.11 0 0
CUI: C1854113
Disease: Prominent nasal bridge
Prominent nasal bridge 		180 8 24 0.11 2 8.3E-02
CUI: C0036508
Disease: Seborrheic dermatitis
Seborrheic dermatitis 		39 0 10 0.10 0 0
CUI: C3164445
Disease: Abnormality of aortic valve
Abnormality of aortic valve 		50 0 11 0.10 0 0
CUI: C0158734
Disease: Polydactyly of toes
Polydactyly of toes 		61 0 12 0.10 0 0
CUI: C4021797
Disease: Abnormality of the thorax
Abnormality of the thorax 		40 0 10 0.10 0 0
CUI: C2936346
Disease: 22q11 Deletion Syndrome
22q11 Deletion Syndrome 		31 0 9 0.10 0 0
CUI: C0685891
Disease: Congenital hypoplasia of thymus
Congenital hypoplasia of thymus 		34 0 9 9.8E-02 0 0
CUI: C0220704
Disease: Shprintzen syndrome
Shprintzen syndrome 		46 0 10 9.7E-02 0 0
CUI: C0240538
Disease: Convex nasal ridge
Convex nasal ridge 		69 8 12 9.7E-02 1 4.0E-02
CUI: C1861324
Disease: Short philtrum
Short philtrum 		182 25 21 9.2E-02 1 2.4E-02
CUI: C0240543
Disease: Bulbous nose
Bulbous nose 		123 13 16 9.2E-02 1 3.3E-02
CUI: C0034150
Disease: Purpura
Purpura 		68 0 11 8.9E-02 0 0
CUI: C0566620
Disease: Nasal voice
Nasal voice 		93 0 13 8.8E-02 0 0
CUI: C0546967
Disease: Posterior embryotoxon
Posterior embryotoxon 		44 0 9 8.8E-02 0 0
CUI: C0004368
Disease: Autoimmune state
Autoimmune state 		70 0 11 8.7E-02 0 0
CUI: C0431718
Disease: Multiple renal cysts
Multiple renal cysts 		46 0 9 8.7E-02 0 0
CUI: C0015732
Disease: Fecal Incontinence
Fecal Incontinence 		60 0 10 8.5E-02 0 0
CUI: C2674608
Disease: Feeding difficulties in infancy
Feeding difficulties in infancy 		305 22 29 8.5E-02 2 5.3E-02
CUI: C0003466
Disease: Anus, Imperforate
Anus, Imperforate 		139 0 16 8.4E-02 0 0
CUI: C0041207
Disease: Truncus Arteriosus, Persistent
Truncus Arteriosus, Persistent 		76 0 11 8.3E-02 0 0
CUI: C0973461
Disease: Dysphasia
Dysphasia 		63 0 10 8.3E-02 0 0
CUI: C1851792
Disease: Aplasia/Hypoplasia of the earlobes
Aplasia/Hypoplasia of the earlobes 		11 0 6 8.3E-02 0 0