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: C0001193
Disease: Apert syndrome
Apert syndrome 		1 14 1 3.8E-02 1 6.1E-03
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma 		1 0 1 3.8E-02 0 0
CUI: C0008073
Disease: Developmental Disabilities
Developmental Disabilities 		1 0 1 3.8E-02 0 0
CUI: C0009451
Disease: Communicating Hydrocephalus
Communicating Hydrocephalus 		1 0 1 3.8E-02 0 0
CUI: C0014866
Disease: Esophageal Stenosis
Esophageal Stenosis 		1 0 1 3.8E-02 0 0
CUI: C0024221
Disease: Lymphangioma
Lymphangioma 		1 0 1 3.8E-02 0 0
CUI: C0030521
Disease: Parathyroid Neoplasms
Parathyroid Neoplasms 		1 2 1 3.8E-02 2 1.3E-02
CUI: C0033141
Disease: Cardiomyopathies, Primary
Cardiomyopathies, Primary 		1 1 1 3.8E-02 1 6.6E-03
CUI: C0037284
Disease: Skin lesion
Skin lesion 		1 0 1 3.8E-02 0 0
CUI: C0040128
Disease: Thyroid Diseases
Thyroid Diseases 		1 0 1 3.8E-02 0 0
CUI: C0040137
Disease: Thyroid Nodule
Thyroid Nodule 		1 5 1 3.8E-02 1 6.4E-03
CUI: C0041657
Disease: Unconscious State
Unconscious State 		1 0 1 3.8E-02 0 0
CUI: C0152207
Disease: Alternating Exotropia
Alternating Exotropia 		1 0 1 3.8E-02 0 0
CUI: C0154828
Disease: Traction detachment of retina
Traction detachment of retina 		1 0 1 3.8E-02 0 0
CUI: C0158763
Disease: Macrodactylia of fingers
Macrodactylia of fingers 		1 1 1 3.8E-02 1 6.6E-03
CUI: C0158768
Disease: Macrodactyly of toe
Macrodactyly of toe 		1 1 1 3.8E-02 1 6.6E-03
CUI: C0205770
Disease: Choroid Plexus Papilloma
Choroid Plexus Papilloma 		1 7 1 3.8E-02 2 1.3E-02
CUI: C0206620
Disease: Lymphangioma, Cystic
Lymphangioma, Cystic 		1 0 1 3.8E-02 0 0
CUI: C0221273
Disease: Juvenile polyp
Juvenile polyp 		1 0 1 3.8E-02 0 0
CUI: C0238461
Disease: Anaplastic thyroid carcinoma
Anaplastic thyroid carcinoma 		1 1 1 3.8E-02 1 6.6E-03
CUI: C0238506
Disease: Congenital posterior urethral valves
Congenital posterior urethral valves 		1 0 1 3.8E-02 0 0
CUI: C0239803
Disease: Red hair
Red hair 		1 0 1 3.8E-02 0 0
CUI: C0265326
Disease: Bannayan-Riley-Ruvalcaba Syndrome
Bannayan-Riley-Ruvalcaba Syndrome 		1 0 1 3.8E-02 0 0
CUI: C0265552
Disease: Congenital macrodactylia
Congenital macrodactylia 		1 1 1 3.8E-02 1 6.6E-03
CUI: C0266166
Disease: Congenital duplication of intestine
Congenital duplication of intestine 		1 1 1 3.8E-02 1 6.6E-03