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: C1831619
Disease: Phosphaturic Mesenchymal Tumor
Phosphaturic Mesenchymal Tumor 		6 0 3 0.50 0 0
CUI: C0030470
Disease: Paranasal Sinus Neoplasms
Paranasal Sinus Neoplasms 		1 0 1 0.33 0 0
CUI: C0240515
Disease: Nipple pain
Nipple pain 		1 0 1 0.33 0 0
CUI: C0263981
Disease: Massive calcification in paraplegic
Massive calcification in paraplegic 		1 0 1 0.33 0 0
CUI: C0341422
Disease: Non-occlusive mesenteric ischemia
Non-occlusive mesenteric ischemia 		1 0 1 0.33 0 0
CUI: C0342653
Disease: Acquired hypophosphatemia
Acquired hypophosphatemia 		1 0 1 0.33 0 0
CUI: C0423637
Disease: Sore nipple
Sore nipple 		1 0 1 0.33 0 0
CUI: C0432149
Disease: Lumbar hemivertebra
Lumbar hemivertebra 		1 0 1 0.33 0 0
CUI: C1333286
Disease: Diencephalic Neoplasm
Diencephalic Neoplasm 		1 0 1 0.33 0 0
CUI: C1845146
Disease: Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate 		1 0 1 0.33 0 0
CUI: C3843745
Disease: Squamous cell (epidermoid) carcinoma
Squamous cell (epidermoid) carcinoma 		1 0 1 0.33 0 0
CUI: C4016104
Disease: HYPOGONADOTROPIC HYPOGONADISM 2 WITH ANOSMIA
HYPOGONADOTROPIC HYPOGONADISM 2 WITH ANOSMIA 		1 0 1 0.33 0 0
CUI: C4330844
Disease: Nutritional Hypophosphatemic Rickets
Nutritional Hypophosphatemic Rickets 		1 0 1 0.33 0 0
CUI: C4693863
Disease: TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2 		1 0 1 0.33 0 0
CUI: C0155912
Disease: Pulmonary Alveolar Microlithiasis
Pulmonary Alveolar Microlithiasis 		2 0 1 0.25 0 0
CUI: C0334067
Disease: Non-Ossifying Fibroma
Non-Ossifying Fibroma 		2 0 1 0.25 0 0
CUI: C0376527
Disease: Skull Base Neoplasms
Skull Base Neoplasms 		2 0 1 0.25 0 0
CUI: C0403566
Disease: Adynamic bone disease
Adynamic bone disease 		2 0 1 0.25 0 0
CUI: C0855056
Disease: Metastatic leiomyosarcoma
Metastatic leiomyosarcoma 		2 0 1 0.25 0 0
CUI: C1336733
Disease: Thalamic Neoplasm
Thalamic Neoplasm 		2 0 1 0.25 0 0
CUI: C1442839
Disease: Hypervitaminosis D
Hypervitaminosis D 		2 0 1 0.25 0 0
CUI: C1845147
Disease: Hypoplasia of the frontal bone
Hypoplasia of the frontal bone 		2 0 1 0.25 0 0
CUI: C1852406
Disease: Cutis Gyrata Syndrome of Beare And Stevenson
Cutis Gyrata Syndrome of Beare And Stevenson 		2 0 1 0.25 0 0
CUI: C1853256
Disease: Hyperostosis-hyperphosphatemia syndrome
Hyperostosis-hyperphosphatemia syndrome 		2 0 1 0.25 0 0
CUI: C1863363
Disease: Cartilaginous trachea
Cartilaginous trachea 		2 0 1 0.25 0 0