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: C4551951
Disease: Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1
Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1 		8 0 1 0.12 0 0
CUI: C1833662
Disease: INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA 		34 0 1 2.9E-02 0 0
CUI: C0007121
Disease: Bronchogenic Carcinoma
Bronchogenic Carcinoma 		47 0 1 2.1E-02 0 0
CUI: C0006663
Disease: Calcinosis
Calcinosis 		52 0 1 1.9E-02 0 0
CUI: C0279593
Disease: Adult B Acute Lymphoblastic Leukemia
Adult B Acute Lymphoblastic Leukemia 		74 0 1 1.4E-02 0 0
CUI: C0349636
Disease: Pre B-cell acute lymphoblastic leukemia
Pre B-cell acute lymphoblastic leukemia 		90 0 1 1.1E-02 0 0
CUI: C0266295
Disease: Congenital hypoplasia of kidney
Congenital hypoplasia of kidney 		96 0 1 1.0E-02 0 0
CUI: C0279584
Disease: Childhood B Acute Lymphoblastic Leukemia
Childhood B Acute Lymphoblastic Leukemia 		99 0 1 1.0E-02 0 0
CUI: C0009691
Disease: Congenital cataract
Congenital cataract 		105 104 1 9.5E-03 1 9.6E-03
CUI: C0266999
Disease: Vesicular Stomatitis
Vesicular Stomatitis 		112 0 1 8.9E-03 0 0
CUI: C1277241
Disease: Delayed myelination
Delayed myelination 		112 0 1 8.9E-03 0 0
CUI: C1837397
Disease: Severe global developmental delay
Severe global developmental delay 		130 0 1 7.7E-03 0 0
CUI: C0029401
Disease: Osteitis Deformans
Osteitis Deformans 		134 0 1 7.5E-03 0 0
CUI: C0024408
Disease: Machado-Joseph Disease
Machado-Joseph Disease 		135 0 1 7.4E-03 0 0
CUI: C0231341
Disease: Premature aging syndrome
Premature aging syndrome 		136 0 1 7.4E-03 0 0
CUI: C4551649
Disease: Congenital Dysplasia Of The Hip
Congenital Dysplasia Of The Hip 		147 0 1 6.8E-03 0 0
CUI: C1285162
Disease: Degenerative disorder
Degenerative disorder 		160 0 1 6.3E-03 0 0
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding) 		160 246 1 6.3E-03 1 4.1E-03
CUI: C1836038
Disease: Poor head control
Poor head control 		162 0 1 6.2E-03 0 0
CUI: C0236642
Disease: Pick Disease of the Brain
Pick Disease of the Brain 		213 0 1 4.7E-03 0 0
CUI: C1843013
Disease: Alzheimer disease, familial, type 3
Alzheimer disease, familial, type 3 		213 0 1 4.7E-03 0 0
CUI: C1854882
Disease: Absent speech
Absent speech 		232 0 1 4.3E-03 0 0
CUI: C0014378
Disease: Enterovirus Infections
Enterovirus Infections 		237 0 1 4.2E-03 0 0
CUI: C0020295
Disease: Hydronephrosis
Hydronephrosis 		253 0 1 4.0E-03 0 0
CUI: C0751690
Disease: Malignant Peripheral Nerve Sheath Tumor
Malignant Peripheral Nerve Sheath Tumor 		261 0 1 3.8E-03 0 0