Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Pectus excavatum of inferior sternum
5 0 4 0.67 0 0
CUI: C4024692
Disease: Reduced factor XIII activity
Reduced factor XIII activity
5 0 3 0.43 0 0
CUI: C0700199
Disease: Multiple nevi
Multiple nevi
2 0 2 0.40 0 0
CUI: C4551484
Disease: Leopard Syndrome 1
Leopard Syndrome 1
6 0 3 0.38 0 0
CUI: C0398639
Disease: Amegakaryocytic thrombocytopenia
Amegakaryocytic thrombocytopenia
7 0 3 0.33 0 0
CUI: C0043324
Disease: Juvenile Xanthogranuloma
Juvenile Xanthogranuloma
4 0 2 0.29 0 0
CUI: C2931482
Disease: Neurofibromatosis-Noonan syndrome
Neurofibromatosis-Noonan syndrome
4 0 2 0.29 0 0
CUI: C0457179
Disease: Desmoplastic infantile astrocytoma
Desmoplastic infantile astrocytoma
5 0 2 0.25 0 0
CUI: C0917817
Disease: Neurofibromatosis 3
Neurofibromatosis 3
5 0 2 0.25 0 0
CUI: C4073145
Disease: Hyperkeratosis pilaris
Hyperkeratosis pilaris
5 0 2 0.25 0 0
CUI: C0041409
Disease: Turner Syndrome, Male
Turner Syndrome, Male
11 0 3 0.23 0 0
CUI: C1527404
Disease: Female Pseudo-Turner Syndrome
Female Pseudo-Turner Syndrome
11 0 3 0.23 0 0
CUI: C1834124
Disease: Shield chest
Shield chest
12 0 3 0.21 0 0
CUI: C0009761
Disease: Conjunctival Neoplasms
Conjunctival Neoplasms
1 0 1 0.20 0 0
CUI: C0035290
Disease: Reticulohistiocytic granuloma
Reticulohistiocytic granuloma
1 0 1 0.20 0 0
CUI: C0152190
Disease: Refractive amblyopia
Refractive amblyopia
1 0 1 0.20 0 0
Congenital stenosis of pulmonary valve
1 0 1 0.20 0 0
CUI: C0162504
Disease: Neutrophilic Eccrine Hidradenitis
Neutrophilic Eccrine Hidradenitis
1 0 1 0.20 0 0
CUI: C0239894
Disease: HEART DISPLACEMENT
HEART DISPLACEMENT
1 0 1 0.20 0 0
Congenital insufficiency of pulmonary valve
1 0 1 0.20 0 0
CUI: C0278600
Disease: Childhood Brain Stem Glioma
Childhood Brain Stem Glioma
1 0 1 0.20 0 0
CUI: C0302323
Disease: Reticulohistiocytosis
Reticulohistiocytosis
1 0 1 0.20 0 0
CUI: C0332881
Disease: Congenital pseudoarthrosis
Congenital pseudoarthrosis
1 0 1 0.20 0 0
CUI: C0334467
Disease: Fibrolipoma
Fibrolipoma
1 0 1 0.20 0 0
CUI: C0349533
Disease: Lymphoma of intestine
Lymphoma of intestine
1 0 1 0.20 0 0