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: C0007871
Disease: Uterine Cervical Incompetence
Uterine Cervical Incompetence 		1 0 1 2.1E-02 0 0
CUI: C0009761
Disease: Conjunctival Neoplasms
Conjunctival Neoplasms 		1 0 1 2.1E-02 0 0
CUI: C0030215
Disease: Palatal Neoplasms
Palatal Neoplasms 		1 0 1 2.1E-02 0 0
CUI: C0035290
Disease: Reticulohistiocytic granuloma
Reticulohistiocytic granuloma 		1 0 1 2.1E-02 0 0
CUI: C0152091
Disease: Osteochondropathy
Osteochondropathy 		1 0 1 2.1E-02 0 0
CUI: C0153470
Disease: Malignant neoplasm of spleen
Malignant neoplasm of spleen 		1 0 1 2.1E-02 0 0
CUI: C0162504
Disease: Neutrophilic Eccrine Hidradenitis
Neutrophilic Eccrine Hidradenitis 		1 0 1 2.1E-02 0 0
CUI: C0238590
Disease: Acrogeria
Acrogeria 		1 0 1 2.1E-02 0 0
CUI: C0271618
Disease: Delayed female puberty
Delayed female puberty 		1 0 1 2.1E-02 0 0
CUI: C0278600
Disease: Childhood Brain Stem Glioma
Childhood Brain Stem Glioma 		1 0 1 2.1E-02 0 0
CUI: C0302323
Disease: Reticulohistiocytosis
Reticulohistiocytosis 		1 0 1 2.1E-02 0 0
CUI: C0339352
Disease: Capsular cataract (disorder)
Capsular cataract (disorder) 		1 0 1 2.1E-02 0 0
CUI: C0340649
Disease: Dissection of iliac artery
Dissection of iliac artery 		1 0 1 2.1E-02 0 0
CUI: C0343079
Disease: Milia, Multiple Eruptive
Milia, Multiple Eruptive 		1 0 1 2.1E-02 0 0
CUI: C0343114
Disease: Woolly hair nevus
Woolly hair nevus 		1 0 1 2.1E-02 0 0
CUI: C0344544
Disease: Polycoria
Polycoria 		1 0 1 2.1E-02 0 0
CUI: C0345382
Disease: Gorlin Chaudhry Moss syndrome
Gorlin Chaudhry Moss syndrome 		1 0 1 2.1E-02 0 0
CUI: C0349533
Disease: Lymphoma of intestine
Lymphoma of intestine 		1 0 1 2.1E-02 0 0
CUI: C0406584
Disease: Acrogeria, gottron type
Acrogeria, gottron type 		1 0 1 2.1E-02 0 0
CUI: C0431501
Disease: Bilateral arterial duct
Bilateral arterial duct 		1 1 1 2.1E-02 1 0.50
CUI: C0432125
Disease: Bicoronal craniosynostosis
Bicoronal craniosynostosis 		1 0 1 2.1E-02 0 0
CUI: C0432233
Disease: Trichorhinophalangeal dysplasia type I
Trichorhinophalangeal dysplasia type I 		1 0 1 2.1E-02 0 0
CUI: C0432269
Disease: Lenz Majewski hyperostotic dwarfism
Lenz Majewski hyperostotic dwarfism 		1 0 1 2.1E-02 0 0
CUI: C0432334
Disease: Inherited cutis laxa
Inherited cutis laxa 		1 0 1 2.1E-02 0 0
CUI: C0521579
Disease: Congenital strabismus
Congenital strabismus 		1 0 1 2.1E-02 0 0