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: C0016064
Disease: Fibrous Dysplasia, Monostotic
Fibrous Dysplasia, Monostotic 		1 0 1 0.14 0 0
CUI: C0265593
Disease: Brachymetacarpia
Brachymetacarpia 		1 0 1 0.14 0 0
CUI: C0281952
Disease: Pseudohypothyroidism
Pseudohypothyroidism 		1 0 1 0.14 0 0
CUI: C0340235
Disease: Bronchobiliary fistula
Bronchobiliary fistula 		1 0 1 0.14 0 0
CUI: C0400847
Disease: Ileal Stenosis
Ileal Stenosis 		1 0 1 0.14 0 0
CUI: C0400978
Disease: Secondary sclerosing cholangitis
Secondary sclerosing cholangitis 		1 0 1 0.14 0 0
CUI: C0519055
Disease: Renal involvement in scleroderma
Renal involvement in scleroderma 		1 0 1 0.14 0 0
CUI: C0948048
Disease: Malignant neoplasm progression
Malignant neoplasm progression 		1 0 1 0.14 0 0
CUI: C1275718
Disease: Granulomatous rosacea
Granulomatous rosacea 		1 0 1 0.14 0 0
CUI: C1301260
Disease: Gastrointestinal Crohn's disease
Gastrointestinal Crohn's disease 		1 0 1 0.14 0 0
CUI: C1707332
Disease: Cellular Myxoma
Cellular Myxoma 		1 0 1 0.14 0 0
CUI: C1836122
Disease: SARCOIDOSIS, EARLY-ONSET
SARCOIDOSIS, EARLY-ONSET 		1 0 1 0.14 0 0
CUI: C1858626
Disease: Bicarbonate-wasting renal tubular acidosis
Bicarbonate-wasting renal tubular acidosis 		1 0 1 0.14 0 0
CUI: C1858628
Disease: Increased red cell osmotic resistance
Increased red cell osmotic resistance 		1 0 1 0.14 0 0
CUI: C1861627
Disease: Butterfly vertebral arch
Butterfly vertebral arch 		1 0 1 0.14 0 0
CUI: C1866053
Disease: Deafness, Congenital Heart Defects, and Posterior Embryotoxon
Deafness, Congenital Heart Defects, and Posterior Embryotoxon 		1 0 1 0.14 0 0
CUI: C1970309
Disease: Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation
Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation 		1 0 1 0.14 0 0
CUI: C2675113
Disease: CROHN DISEASE-ASSOCIATED GROWTH FAILURE, SUSCEPTIBILITY TO (finding)
CROHN DISEASE-ASSOCIATED GROWTH FAILURE, SUSCEPTIBILITY TO (finding) 		1 0 1 0.14 0 0
CUI: C2675383
Disease: POLYOSTOTIC FIBROUS DYSPLASIA, SOMATIC, MOSAIC
POLYOSTOTIC FIBROUS DYSPLASIA, SOMATIC, MOSAIC 		1 0 1 0.14 0 0
CUI: C2749995
Disease: Intermittent generalized erythematous papular rash
Intermittent generalized erythematous papular rash 		1 0 1 0.14 0 0
CUI: C4016140
Disease: PSEUDOHYPOPARATHYROIDISM, TYPE IA, WITH TESTOTOXICOSIS
PSEUDOHYPOPARATHYROIDISM, TYPE IA, WITH TESTOTOXICOSIS 		1 0 1 0.14 0 0
CUI: C4016657
Disease: SYSTEMIC LUPUS ERYTHEMATOSUS, ASSOCIATION WITH SUSCEPTIBILITY TO, 2
SYSTEMIC LUPUS ERYTHEMATOSUS, ASSOCIATION WITH SUSCEPTIBILITY TO, 2 		1 0 1 0.14 0 0
CUI: C4024097
Disease: Broad 1st metacarpal
Broad 1st metacarpal 		1 0 1 0.14 0 0
CUI: C4540135
Disease: PITUITARY ADENOMA 3, MULTIPLE TYPES
PITUITARY ADENOMA 3, MULTIPLE TYPES 		1 0 1 0.14 0 0
CUI: C4540536
Disease: PITUITARY TUMOR 3, GROWTH HORMONE-SECRETING, SOMATIC
PITUITARY TUMOR 3, GROWTH HORMONE-SECRETING, SOMATIC 		1 0 1 0.14 0 0