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: C4721207
Disease: Metastatic gastroesophageal adenocarcinoma
Metastatic gastroesophageal adenocarcinoma 		1 0 1 0.14 0 0
CUI: C4725030
Disease: Refractory Nasopharyngeal Carcinoma
Refractory Nasopharyngeal Carcinoma 		1 0 1 0.14 0 0
CUI: C0085569
Disease: Metabolic acidosis, NAG, acidifying salts
Metabolic acidosis, NAG, acidifying salts 		2 0 1 0.12 0 0
CUI: C0235329
Disease: Small bowel obstruction
Small bowel obstruction 		2 0 1 0.12 0 0
CUI: C0341268
Disease: Disorder of small intestine
Disorder of small intestine 		2 0 1 0.12 0 0
CUI: C0342346
Disease: Pseudohypoparathyroidism and pseudopseudohypoparathyroidism
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism 		2 0 1 0.12 0 0
CUI: C0344975
Disease: Pulmonary Atresia with Intact Ventricular Septum
Pulmonary Atresia with Intact Ventricular Septum 		2 0 1 0.12 0 0
CUI: C0405469
Disease: Granulomatous Mastitis
Granulomatous Mastitis 		2 0 1 0.12 0 0
CUI: C0581359
Disease: Acute intestinal obstruction
Acute intestinal obstruction 		2 0 1 0.12 0 0
CUI: C0796000
Disease: Multiple non-ossifying fibromatosis
Multiple non-ossifying fibromatosis 		2 0 1 0.12 0 0
CUI: C1277259
Disease: Pangastritis
Pangastritis 		2 0 1 0.12 0 0
CUI: C1333119
Disease: Colorectal Villous Adenoma
Colorectal Villous Adenoma 		2 0 1 0.12 0 0
CUI: C1610637
Disease: Granulomatous infection
Granulomatous infection 		2 0 1 0.12 0 0
CUI: C1709780
Disease: Pyloric Gland Adenoma
Pyloric Gland Adenoma 		2 0 1 0.12 0 0
CUI: C1710140
Disease: Sparsely Granulated Somatotroph Adenoma
Sparsely Granulated Somatotroph Adenoma 		2 0 1 0.12 0 0
CUI: C1835223
Disease: PSORIATIC ARTHRITIS, SUSCEPTIBILITY TO (finding)
PSORIATIC ARTHRITIS, SUSCEPTIBILITY TO (finding) 		2 0 1 0.12 0 0
CUI: C1849409
Disease: Knobloch syndrome
Knobloch syndrome 		2 0 1 0.12 0 0
CUI: C1850631
Disease: Short 3rd metacarpal
Short 3rd metacarpal 		2 0 1 0.12 0 0
CUI: C1857761
Disease: Alagille Syndrome 2
Alagille Syndrome 2 		2 0 1 0.12 0 0
CUI: C1863184
Disease: Choroid plexus calcification
Choroid plexus calcification 		2 0 1 0.12 0 0
CUI: C1956125
Disease: Alagille Syndrome 1
Alagille Syndrome 1 		2 0 1 0.12 0 0
CUI: C2930797
Disease: Hepatic ductular hypoplasia
Hepatic ductular hypoplasia 		2 0 1 0.12 0 0
CUI: C3554462
Disease: MITOCHONDRIAL DNA DEPLETION SYNDROME 11
MITOCHONDRIAL DNA DEPLETION SYNDROME 11 		2 0 1 0.12 0 0
CUI: C3697137
Disease: Fibrous dysplasia of bone with intramuscular myxoma
Fibrous dysplasia of bone with intramuscular myxoma 		2 0 1 0.12 0 0
CUI: C3805239
Disease: Mid aortic syndrome
Mid aortic syndrome 		2 0 1 0.12 0 0