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: C0206649
Disease: Neoplasms, Fibroepithelial
Neoplasms, Fibroepithelial 		1 0 1 0.33 0 0
CUI: C1389473
Disease: Pelvic hypoplasia
Pelvic hypoplasia 		1 0 1 0.33 0 0
CUI: C1833693
Disease: Otodental Dysplasia
Otodental Dysplasia 		1 0 1 0.33 0 0
CUI: C1834013
Disease: Odontoma dysphagia syndrome
Odontoma dysphagia syndrome 		1 0 1 0.33 0 0
CUI: C1850040
Disease: Pelviscapular dysplasia
Pelviscapular dysplasia 		1 0 1 0.33 0 0
CUI: C1850043
Disease: Anterior rounding of vertebral bodies
Anterior rounding of vertebral bodies 		1 0 1 0.33 0 0
CUI: C3698541
Disease: Ohdo syndrome, Maat-Kievit-Brunner type
Ohdo syndrome, Maat-Kievit-Brunner type 		1 0 1 0.33 0 0
CUI: C4022856
Disease: Skewed maternal X inactivation
Skewed maternal X inactivation 		1 0 1 0.33 0 0
CUI: C4025491
Disease: Abnormality of the joint spaces of the elbow
Abnormality of the joint spaces of the elbow 		1 0 1 0.33 0 0
CUI: C4025862
Disease: Abnormality of the maxilla
Abnormality of the maxilla 		1 0 1 0.33 0 0
CUI: C4511806
Disease: Mitotically active leiomyoma
Mitotically active leiomyoma 		1 0 1 0.33 0 0
CUI: C0038368
Disease: Stomatognathic Diseases
Stomatognathic Diseases 		2 0 1 0.25 0 0
CUI: C0266604
Disease: Congenital aplasia of inner ear
Congenital aplasia of inner ear 		2 0 1 0.25 0 0
CUI: C0267785
Disease: Leiomyomatosis peritonealis disseminata
Leiomyomatosis peritonealis disseminata 		2 0 1 0.25 0 0
CUI: C0855056
Disease: Metastatic leiomyosarcoma
Metastatic leiomyosarcoma 		2 0 1 0.25 0 0
CUI: C1850044
Disease: Prominent protruding coccyx
Prominent protruding coccyx 		2 0 1 0.25 0 0
CUI: C1850048
Disease: Absent proximal finger flexion creases
Absent proximal finger flexion creases 		2 0 1 0.25 0 0
CUI: C1970777
Disease: Abnormally folded helix
Abnormally folded helix 		2 0 1 0.25 0 0
CUI: C2750325
Disease: Oculootodental syndrome
Oculootodental syndrome 		2 0 1 0.25 0 0
CUI: C4022486
Disease: Clinodactyly of the 2nd finger
Clinodactyly of the 2nd finger 		2 0 1 0.25 0 0
CUI: C4023566
Disease: Agenesis of premolar
Agenesis of premolar 		2 0 1 0.25 0 0
CUI: C4025124
Disease: Limited elbow extension and supination
Limited elbow extension and supination 		2 0 1 0.25 0 0
CUI: C4025688
Disease: Abnormality of the skull base
Abnormality of the skull base 		2 0 1 0.25 0 0
CUI: C0028882
Disease: Odontoma
Odontoma 		3 0 1 0.20 0 0
CUI: C0268199
Disease: Familial apolipoprotein C-II deficiency
Familial apolipoprotein C-II deficiency 		3 0 1 0.20 0 0