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: C0002897
Disease: Anemia, Splenic
Anemia, Splenic 		1 0 1 6.2E-02 0 0
CUI: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect 		1 0 1 6.2E-02 0 0
CUI: C0010334
Disease: Crisscross Heart
Crisscross Heart 		1 0 1 6.2E-02 0 0
CUI: C0023869
Disease: Lithiasis
Lithiasis 		1 0 1 6.2E-02 0 0
CUI: C0043379
Disease: XYY Karyotype
XYY Karyotype 		1 0 1 6.2E-02 0 0
CUI: C0232259
Disease: Mid-systolic murmur
Mid-systolic murmur 		1 0 1 6.2E-02 0 0
CUI: C0263579
Disease: Pigmented hairy epidermal nevus
Pigmented hairy epidermal nevus 		1 0 1 6.2E-02 0 0
CUI: C0271586
Disease: Prolactin Deficiency, Isolated
Prolactin Deficiency, Isolated 		1 0 1 6.2E-02 0 0
CUI: C0341037
Disease: Lateral developmental cyst of jaw
Lateral developmental cyst of jaw 		1 0 1 6.2E-02 0 0
CUI: C0342151
Disease: Congenital hypothyroidism without goiter
Congenital hypothyroidism without goiter 		1 0 1 6.2E-02 0 0
CUI: C0342154
Disease: Congenital atrophy of thyroid
Congenital atrophy of thyroid 		1 0 1 6.2E-02 0 0
CUI: C0349477
Disease: Transient neonatal hypothyroidism
Transient neonatal hypothyroidism 		1 0 1 6.2E-02 0 0
CUI: C0409939
Disease: Osteoarthritis of glenohumeral joint
Osteoarthritis of glenohumeral joint 		1 0 1 6.2E-02 0 0
CUI: C0432361
Disease: Diffuse neurofibroma
Diffuse neurofibroma 		1 0 1 6.2E-02 0 0
CUI: C0495452
Disease: Noninfective neonatal diarrhea
Noninfective neonatal diarrhea 		1 0 1 6.2E-02 0 0
CUI: C0553668
Disease: Labored breathing
Labored breathing 		1 0 1 6.2E-02 0 0
CUI: C0856836
Disease: Systemic juvenile chronic arthritis
Systemic juvenile chronic arthritis 		1 0 1 6.2E-02 0 0
CUI: C0948109
Disease: Idiopathic neutropenia
Idiopathic neutropenia 		1 0 1 6.2E-02 0 0
CUI: C1834056
Disease: Thin anteverted nares
Thin anteverted nares 		1 0 1 6.2E-02 0 0
CUI: C1834057
Disease: Vertebral hyperostosis
Vertebral hyperostosis 		1 0 1 6.2E-02 0 0
CUI: C1846331
Disease: Juvenile-onset dystonia
Juvenile-onset dystonia 		1 0 1 6.2E-02 0 0
CUI: C1853100
Disease: CEREBROOCULOFACIOSKELETAL SYNDROME 4
CEREBROOCULOFACIOSKELETAL SYNDROME 4 		1 0 1 6.2E-02 0 0
CUI: C1857508
Disease: Patchy sclerosis of finger phalanx
Patchy sclerosis of finger phalanx 		1 0 1 6.2E-02 0 0
CUI: C1858042
Disease: Becker Nevus Syndrome
Becker Nevus Syndrome 		1 0 1 6.2E-02 0 0
CUI: C1861366
Disease: SYNDACTYLY, TYPE III
SYNDACTYLY, TYPE III 		1 0 1 6.2E-02 0 0