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: C1837203
Disease: WAARDENBURG SYNDROME, TYPE IID
WAARDENBURG SYNDROME, TYPE IID 		1 0 1 0.12 0 0
CUI: C1851988
Disease: Dorsal subluxation of ulna
Dorsal subluxation of ulna 		1 0 1 0.12 0 0
CUI: C1855276
Disease: Dorsolateral bowed, short radii
Dorsolateral bowed, short radii 		1 0 1 0.12 0 0
CUI: C1857652
Disease: Thymic hormone decreased
Thymic hormone decreased 		1 0 1 0.12 0 0
CUI: C2674636
Disease: GASTROINTESTINAL STROMAL TUMOR, FAMILIAL
GASTROINTESTINAL STROMAL TUMOR, FAMILIAL 		1 0 1 0.12 0 0
CUI: C2698309
Disease: B lymphoblastic leukemia lymphoma with t(v;11q23); MLL rearranged
B lymphoblastic leukemia lymphoma with t(v;11q23); MLL rearranged 		1 0 1 0.12 0 0
CUI: C2931518
Disease: Plexosarcoma
Plexosarcoma 		1 0 1 0.12 0 0
CUI: C3151403
Disease: AMYOTROPHIC LATERAL SCLEROSIS 14 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA
AMYOTROPHIC LATERAL SCLEROSIS 14 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 		1 0 1 0.12 0 0
CUI: C3152097
Disease: AMYOTROPHIC LATERAL SCLEROSIS 14 WITHOUT FRONTOTEMPORAL DEMENTIA
AMYOTROPHIC LATERAL SCLEROSIS 14 WITHOUT FRONTOTEMPORAL DEMENTIA 		1 0 1 0.12 0 0
CUI: C3553298
Disease: UV-SENSITIVE SYNDROME 2
UV-SENSITIVE SYNDROME 2 		1 0 1 0.12 0 0
CUI: C3809469
Disease: INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 3
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 3 		1 0 1 0.12 0 0
CUI: C4016294
Disease: PIEBALDISM WITH SENSORINEURAL DEAFNESS
PIEBALDISM WITH SENSORINEURAL DEAFNESS 		1 0 1 0.12 0 0
CUI: C4016297
Disease: PIEBALDISM, PROGRESSIVE
PIEBALDISM, PROGRESSIVE 		1 0 1 0.12 0 0
CUI: C4020828
Disease: Increased spinal bone density
Increased spinal bone density 		1 0 1 0.12 0 0
CUI: C4025076
Disease: Abnormality of hand joint mobility
Abnormality of hand joint mobility 		1 0 1 0.12 0 0
CUI: C4025460
Disease: Broad ulna
Broad ulna 		1 0 1 0.12 0 0
CUI: C4025745
Disease: Abnormal metatarsal morphology
Abnormal metatarsal morphology 		1 0 1 0.12 0 0
CUI: C4038952
Disease: Metastatic thymic carcinoma
Metastatic thymic carcinoma 		1 0 1 0.12 0 0
CUI: C4040134
Disease: Metastatic seminoma
Metastatic seminoma 		1 0 1 0.12 0 0
CUI: C4225244
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Y
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Y 		1 0 1 0.12 0 0
CUI: C4225578
Disease: CHARCOT-MARIE-TOOTH DISEASE, TYPE 2Y
CHARCOT-MARIE-TOOTH DISEASE, TYPE 2Y 		1 0 1 0.12 0 0
CUI: C4267893
Disease: Monoclonal mast cell activation syndrome
Monoclonal mast cell activation syndrome 		1 0 1 0.12 0 0
CUI: C4509020
Disease: Isolated bone marrow mastocytosis
Isolated bone marrow mastocytosis 		1 0 1 0.12 0 0
CUI: C4551978
Disease: Short forearm
Short forearm 		1 0 1 0.12 0 0
CUI: C4706613
Disease: SHOX-related short stature
SHOX-related short stature 		1 0 1 0.12 0 0