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: C0152091
Disease: Osteochondropathy
Osteochondropathy 		1 0 1 3.7E-02 0 0
CUI: C0155930
Disease: Tooth Ankylosis
Tooth Ankylosis 		1 0 1 3.7E-02 0 0
CUI: C0231450
Disease: Abnormal extension
Abnormal extension 		1 0 1 3.7E-02 0 0
CUI: C0265263
Disease: Femoral hypoplasia - unusual facies syndrome
Femoral hypoplasia - unusual facies syndrome 		1 0 1 3.7E-02 0 0
CUI: C0265273
Disease: Achondrogenesis type 1A
Achondrogenesis type 1A 		1 0 1 3.7E-02 0 0
CUI: C0265856
Disease: Hypoplasia of right heart
Hypoplasia of right heart 		1 0 1 3.7E-02 0 0
CUI: C0271869
Disease: Pseudohypoparathyroidism type I B
Pseudohypoparathyroidism type I B 		1 0 1 3.7E-02 0 0
CUI: C0282643
Disease: Smith-Lemli-Opitz Syndrome, Type I
Smith-Lemli-Opitz Syndrome, Type I 		1 0 1 3.7E-02 0 0
CUI: C0282644
Disease: Smith-Lemli-Opitz Syndrome, Type II
Smith-Lemli-Opitz Syndrome, Type II 		1 0 1 3.7E-02 0 0
CUI: C0332885
Disease: Congenital stenosis
Congenital stenosis 		1 0 1 3.7E-02 0 0
CUI: C0340031
Disease: Mucociliary clearance defect
Mucociliary clearance defect 		1 0 1 3.7E-02 0 0
CUI: C0341154
Disease: Esophageal atresia with tracheoesophageal fistula (disorder)
Esophageal atresia with tracheoesophageal fistula (disorder) 		1 0 1 3.7E-02 0 0
CUI: C0375536
Disease: Congenital osteodystrophy
Congenital osteodystrophy 		1 0 1 3.7E-02 0 0
CUI: C0432125
Disease: Bicoronal craniosynostosis
Bicoronal craniosynostosis 		1 0 1 3.7E-02 0 0
CUI: C0685786
Disease: Cleft mandible
Cleft mandible 		1 0 1 3.7E-02 0 0
CUI: C0740850
Disease: airway disease restrictive
airway disease restrictive 		1 0 1 3.7E-02 0 0
CUI: C0743924
Disease: Short fetal femur length
Short fetal femur length 		1 2 1 3.7E-02 2 0.50
CUI: C0748397
Disease: Reynolds syndrome
Reynolds syndrome 		1 0 1 3.7E-02 0 0
CUI: C0877313
Disease: Neonatal neuroblastoma
Neonatal neuroblastoma 		1 0 1 3.7E-02 0 0
CUI: C1300256
Disease: Thanatophoric dysplasia, type 1
Thanatophoric dysplasia, type 1 		1 0 1 3.7E-02 0 0
CUI: C1300260
Disease: Spondyloepimetaphyseal dysplasia, sponastrime type
Spondyloepimetaphyseal dysplasia, sponastrime type 		1 0 1 3.7E-02 0 0
CUI: C1300267
Disease: Brachydactyly syndrome type B
Brachydactyly syndrome type B 		1 0 1 3.7E-02 0 0
CUI: C1389473
Disease: Pelvic hypoplasia
Pelvic hypoplasia 		1 0 1 3.7E-02 0 0
CUI: C1707549
Disease: Cutaneous Lymphomatoid Granulomatosis
Cutaneous Lymphomatoid Granulomatosis 		1 0 1 3.7E-02 0 0
CUI: C1834821
Disease: METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS
METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS 		1 0 1 3.7E-02 0 0