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: C0009761
Disease: Conjunctival Neoplasms
Conjunctival Neoplasms 		1 0 1 2.6E-02 0 0
CUI: C0016064
Disease: Fibrous Dysplasia, Monostotic
Fibrous Dysplasia, Monostotic 		1 0 1 2.6E-02 0 0
CUI: C0035290
Disease: Reticulohistiocytic granuloma
Reticulohistiocytic granuloma 		1 0 1 2.6E-02 0 0
CUI: C0152091
Disease: Osteochondropathy
Osteochondropathy 		1 0 1 2.6E-02 0 0
CUI: C0162504
Disease: Neutrophilic Eccrine Hidradenitis
Neutrophilic Eccrine Hidradenitis 		1 0 1 2.6E-02 0 0
CUI: C0231450
Disease: Abnormal extension
Abnormal extension 		1 0 1 2.6E-02 0 0
CUI: C0232874
Disease: Febrile proteinuria
Febrile proteinuria 		1 0 1 2.6E-02 0 0
CUI: C0233623
Disease: Onychotillomania
Onychotillomania 		1 0 1 2.6E-02 0 0
CUI: C0243057
Disease: Stomatognathic System Abnormalities
Stomatognathic System Abnormalities 		1 0 1 2.6E-02 0 0
CUI: C0264402
Disease: Gas bubble disease
Gas bubble disease 		1 0 1 2.6E-02 0 0
CUI: C0265241
Disease: Franceschetti-Klein syndrome
Franceschetti-Klein syndrome 		1 0 1 2.6E-02 0 0
CUI: C0265248
Disease: Ruvalcaba Syndrome
Ruvalcaba Syndrome 		1 0 1 2.6E-02 0 0
CUI: C0265593
Disease: Brachymetacarpia
Brachymetacarpia 		1 0 1 2.6E-02 0 0
CUI: C0265856
Disease: Hypoplasia of right heart
Hypoplasia of right heart 		1 0 1 2.6E-02 0 0
CUI: C0266878
Disease: External resorption of tooth
External resorption of tooth 		1 0 1 2.6E-02 0 0
CUI: C0276270
Disease: Oral papillomatosis
Oral papillomatosis 		1 0 1 2.6E-02 0 0
CUI: C0278600
Disease: Childhood Brain Stem Glioma
Childhood Brain Stem Glioma 		1 0 1 2.6E-02 0 0
CUI: C0281952
Disease: Pseudohypothyroidism
Pseudohypothyroidism 		1 0 1 2.6E-02 0 0
CUI: C0302323
Disease: Reticulohistiocytosis
Reticulohistiocytosis 		1 0 1 2.6E-02 0 0
CUI: C0349533
Disease: Lymphoma of intestine
Lymphoma of intestine 		1 0 1 2.6E-02 0 0
CUI: C0432125
Disease: Bicoronal craniosynostosis
Bicoronal craniosynostosis 		1 0 1 2.6E-02 0 0
CUI: C0432238
Disease: Bent bone dysplasia
Bent bone dysplasia 		1 0 1 2.6E-02 0 0
CUI: C0432334
Disease: Inherited cutis laxa
Inherited cutis laxa 		1 0 1 2.6E-02 0 0
CUI: C0521579
Disease: Congenital strabismus
Congenital strabismus 		1 0 1 2.6E-02 0 0
CUI: C0578682
Disease: Madarosis of eyebrow
Madarosis of eyebrow 		1 0 1 2.6E-02 0 0