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: C0334393
Disease: Adenocarcinoma with squamous metaplasia
Adenocarcinoma with squamous metaplasia 		1 0 1 1.9E-02 0 0
CUI: C0334491
Disease: Benign Mesenchymoma
Benign Mesenchymoma 		1 0 1 1.9E-02 0 0
CUI: C0344487
Disease: Lateral meningocele
Lateral meningocele 		1 0 1 1.9E-02 0 0
CUI: C0349565
Disease: Lipoma of breast
Lipoma of breast 		1 0 1 1.9E-02 0 0
CUI: C0349623
Disease: Primary Melanocytic Lesion of Meninges
Primary Melanocytic Lesion of Meninges 		1 0 1 1.9E-02 0 0
CUI: C0398709
Disease: Secretory Component Deficiency
Secretory Component Deficiency 		1 0 1 1.9E-02 0 0
CUI: C0425492
Disease: Irregular breathing
Irregular breathing 		1 0 1 1.9E-02 0 0
CUI: C0431124
Disease: Cellular Schwannoma
Cellular Schwannoma 		1 0 1 1.9E-02 0 0
CUI: C0432125
Disease: Bicoronal craniosynostosis
Bicoronal craniosynostosis 		1 0 1 1.9E-02 0 0
CUI: C0432149
Disease: Lumbar hemivertebra
Lumbar hemivertebra 		1 0 1 1.9E-02 0 0
CUI: C0432238
Disease: Bent bone dysplasia
Bent bone dysplasia 		1 0 1 1.9E-02 0 0
CUI: C0432273
Disease: Worth disease
Worth disease 		1 0 1 1.9E-02 0 0
CUI: C0432334
Disease: Inherited cutis laxa
Inherited cutis laxa 		1 0 1 1.9E-02 0 0
CUI: C0495640
Disease: Congenital malformation syndromes involving early overgrowth
Congenital malformation syndromes involving early overgrowth 		1 0 1 1.9E-02 0 0
CUI: C0522035
Disease: Edema of the upper extremity
Edema of the upper extremity 		1 0 1 1.9E-02 0 0
CUI: C0585540
Disease: Myoclonus, Oculopalatal
Myoclonus, Oculopalatal 		1 0 1 1.9E-02 0 0
CUI: C0685678
Disease: Incomplete ossification of pubis
Incomplete ossification of pubis 		1 0 1 1.9E-02 0 0
CUI: C0685732
Disease: Congenital dilatation of pulmonary artery
Congenital dilatation of pulmonary artery 		1 0 1 1.9E-02 0 0
CUI: C0743515
Disease: endometrial polyp benign
endometrial polyp benign 		1 0 1 1.9E-02 0 0
CUI: C0750931
Disease: Arnold-Chiari Malformation, Type III
Arnold-Chiari Malformation, Type III 		1 0 1 1.9E-02 0 0
CUI: C0750932
Disease: Arnold-Chiari Malformation, Type IV
Arnold-Chiari Malformation, Type IV 		1 0 1 1.9E-02 0 0
CUI: C0751348
Disease: Myoclonus Simplex
Myoclonus Simplex 		1 0 1 1.9E-02 0 0
CUI: C0751350
Disease: Myoclonus, Lower Extremity
Myoclonus, Lower Extremity 		1 0 1 1.9E-02 0 0
CUI: C0751351
Disease: Myoclonus, Segmental
Myoclonus, Segmental 		1 0 1 1.9E-02 0 0
CUI: C0751352
Disease: Myoclonus, Nocturnal
Myoclonus, Nocturnal 		1 0 1 1.9E-02 0 0