Source: CLINVAR ×
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: C0008073
Disease: Developmental Disabilities
Developmental Disabilities 		1 0 1 7.7E-02 0 0
CUI: C0021933
Disease: Intussusception
Intussusception 		1 0 1 7.7E-02 0 0
CUI: C0024221
Disease: Lymphangioma
Lymphangioma 		1 0 1 7.7E-02 0 0
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome 		1 0 1 7.7E-02 0 0
CUI: C0033141
Disease: Cardiomyopathies, Primary
Cardiomyopathies, Primary 		1 0 1 7.7E-02 0 0
CUI: C0033578
Disease: Prostatic Neoplasms
Prostatic Neoplasms 		1 1 1 7.7E-02 1 1.2E-02
CUI: C0037284
Disease: Skin lesion
Skin lesion 		1 0 1 7.7E-02 0 0
CUI: C0040128
Disease: Thyroid Diseases
Thyroid Diseases 		1 0 1 7.7E-02 0 0
CUI: C0040137
Disease: Thyroid Nodule
Thyroid Nodule 		1 5 1 7.7E-02 1 1.2E-02
CUI: C0041657
Disease: Unconscious State
Unconscious State 		1 0 1 7.7E-02 0 0
CUI: C0042138
Disease: Uterine Neoplasms
Uterine Neoplasms 		1 0 1 7.7E-02 0 0
CUI: C0158763
Disease: Macrodactylia of fingers
Macrodactylia of fingers 		1 1 1 7.7E-02 1 1.2E-02
CUI: C0158768
Disease: Macrodactyly of toe
Macrodactyly of toe 		1 1 1 7.7E-02 1 1.2E-02
CUI: C0221273
Disease: Juvenile polyp
Juvenile polyp 		1 0 1 7.7E-02 0 0
CUI: C0239803
Disease: Red hair
Red hair 		1 0 1 7.7E-02 0 0
CUI: C0265326
Disease: Bannayan-Riley-Ruvalcaba Syndrome
Bannayan-Riley-Ruvalcaba Syndrome 		1 0 1 7.7E-02 0 0
CUI: C0265552
Disease: Congenital macrodactylia
Congenital macrodactylia 		1 1 1 7.7E-02 1 1.2E-02
CUI: C0266166
Disease: Congenital duplication of intestine
Congenital duplication of intestine 		1 0 1 7.7E-02 0 0
CUI: C0271618
Disease: Delayed female puberty
Delayed female puberty 		1 0 1 7.7E-02 0 0
CUI: C0343082
Disease: Senile angioma
Senile angioma 		1 0 1 7.7E-02 0 0
CUI: C0343114
Disease: Woolly hair nevus
Woolly hair nevus 		1 0 1 7.7E-02 0 0
CUI: C0431448
Disease: Absent eyebrow
Absent eyebrow 		1 1 1 7.7E-02 1 1.2E-02
CUI: C0457193
Disease: Soft tissue mass
Soft tissue mass 		1 0 1 7.7E-02 0 0
CUI: C0521579
Disease: Congenital strabismus
Congenital strabismus 		1 0 1 7.7E-02 0 0
CUI: C0544862
Disease: Neurocutaneous melanosis
Neurocutaneous melanosis 		1 1 1 7.7E-02 1 1.2E-02