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: C0334036
Disease: Apocrine metaplasia
Apocrine metaplasia 		0 1 0 0 1 0.17
CUI: C0004048
Disease: Inspiration function
Inspiration function 		1 0 1 2.8E-02 0 0
CUI: C0152091
Disease: Osteochondropathy
Osteochondropathy 		1 0 1 2.8E-02 0 0
CUI: C0158538
Disease: Other congenital anomalies of nervous system
Other congenital anomalies of nervous system 		1 0 1 2.8E-02 0 0
CUI: C0158763
Disease: Macrodactylia of fingers
Macrodactylia of fingers 		1 0 1 2.8E-02 0 0
CUI: C0158768
Disease: Macrodactyly of toe
Macrodactyly of toe 		1 1 1 2.8E-02 1 0.17
CUI: C0158784
Disease: Accessory skeletal muscle
Accessory skeletal muscle 		1 0 1 2.8E-02 0 0
CUI: C0262477
Disease: Eye problem
Eye problem 		1 0 1 2.8E-02 0 0
CUI: C0265248
Disease: Ruvalcaba Syndrome
Ruvalcaba Syndrome 		1 0 1 2.8E-02 0 0
CUI: C0276270
Disease: Oral papillomatosis
Oral papillomatosis 		1 0 1 2.8E-02 0 0
CUI: C0278714
Disease: stage IV Wilms tumor
stage IV Wilms tumor 		1 0 1 2.8E-02 0 0
CUI: C0332881
Disease: Congenital pseudoarthrosis
Congenital pseudoarthrosis 		1 0 1 2.8E-02 0 0
CUI: C0334467
Disease: Fibrolipoma
Fibrolipoma 		1 0 1 2.8E-02 0 0
CUI: C0344787
Disease: Complete atrioventricular septal defect
Complete atrioventricular septal defect 		1 0 1 2.8E-02 0 0
CUI: C0346178
Disease: Ovarian gynandroblastoma
Ovarian gynandroblastoma 		1 0 1 2.8E-02 0 0
CUI: C0349538
Disease: Malignant melanoma of anus
Malignant melanoma of anus 		1 0 1 2.8E-02 0 0
CUI: C0432125
Disease: Bicoronal craniosynostosis
Bicoronal craniosynostosis 		1 0 1 2.8E-02 0 0
CUI: C0432360
Disease: Neurofibromatosis type 5
Neurofibromatosis type 5 		1 0 1 2.8E-02 0 0
CUI: C0495640
Disease: Congenital malformation syndromes involving early overgrowth
Congenital malformation syndromes involving early overgrowth 		1 0 1 2.8E-02 0 0
CUI: C0600114
Disease: Testicular stromal tumor
Testicular stromal tumor 		1 0 1 2.8E-02 0 0
CUI: C0749794
Disease: Upper Extremity Deformities, Congenital
Upper Extremity Deformities, Congenital 		1 0 1 2.8E-02 0 0
CUI: C0751679
Disease: Ganglioglioma, Intracranial
Ganglioglioma, Intracranial 		1 0 1 2.8E-02 0 0
CUI: C0752127
Disease: Spinal Cord Vascular Diseases
Spinal Cord Vascular Diseases 		1 0 1 2.8E-02 0 0
CUI: C0795812
Disease: Chromosome 4, trisomy 4q
Chromosome 4, trisomy 4q 		1 0 1 2.8E-02 0 0
CUI: C0795868
Disease: Chromosome 18, tetrasomy 18p
Chromosome 18, tetrasomy 18p 		1 0 1 2.8E-02 0 0