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: C0004048
Disease: Inspiration function
Inspiration function
1 0 1 1.9E-02 0 0
CUI: C0023441
Disease: Leukemia, Experimental
Leukemia, Experimental
1 0 1 1.9E-02 0 0
CUI: C0030215
Disease: Palatal Neoplasms
Palatal Neoplasms
1 0 1 1.9E-02 0 0
CUI: C0037932
Disease: Curvature of spine
Curvature of spine
1 0 1 1.9E-02 0 0
CUI: C0153470
Disease: Malignant neoplasm of spleen
Malignant neoplasm of spleen
1 0 1 1.9E-02 0 0
CUI: C0206649
Disease: Neoplasms, Fibroepithelial
Neoplasms, Fibroepithelial
1 0 1 1.9E-02 0 0
CUI: C0265669
Disease: Congenital dislocation of knee
Congenital dislocation of knee
1 0 1 1.9E-02 0 0
CUI: C0265878
Disease: Preductal coarctation of aorta
Preductal coarctation of aorta
1 0 1 1.9E-02 0 0
CUI: C0268875
Disease: Urethrorectal fistula
Urethrorectal fistula
1 0 1 1.9E-02 0 0
CUI: C0271618
Disease: Delayed female puberty
Delayed female puberty
1 0 1 1.9E-02 0 0
CUI: C0340031
Disease: Mucociliary clearance defect
Mucociliary clearance defect
1 0 1 1.9E-02 0 0
CUI: C0343079
Disease: Milia, Multiple Eruptive
Milia, Multiple Eruptive
1 0 1 1.9E-02 0 0
CUI: C0343114
Disease: Woolly hair nevus
Woolly hair nevus
1 0 1 1.9E-02 0 0
CUI: C0349539
Disease: Malignant melanoma of rectum
Malignant melanoma of rectum
1 0 1 1.9E-02 0 0
CUI: C0429803
Disease: Bladder trabeculation
Bladder trabeculation
1 0 1 1.9E-02 0 0
CUI: C0431691
Disease: Unilateral Renal Hypoplasia
Unilateral Renal Hypoplasia
1 0 1 1.9E-02 0 0
CUI: C0432201
Disease: Boomerang dysplasia
Boomerang dysplasia
1 0 1 1.9E-02 0 0
Other congenital malformations of spine, not associated with scoliosis
1 0 1 1.9E-02 0 0
CUI: C0544862
Disease: Neurocutaneous melanosis
Neurocutaneous melanosis
1 0 1 1.9E-02 0 0
CUI: C0549608
Disease: VEINS/LYMPHATICS
VEINS/LYMPHATICS
1 0 1 1.9E-02 0 0
3-Phosphoglycerate dehydrogenase deficiency
1 0 1 1.9E-02 0 0
CUI: C0740850
Disease: airway disease restrictive
airway disease restrictive
1 0 1 1.9E-02 0 0
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
Deafness, congenital onychodystrophy, recessive form
1 0 1 1.9E-02 0 0